Petition for Inter Partes Review
`Patent No. 9,302,102 B2
`
`
`
`
`
`SALPETER
`EXHIBIT 1018
`
`
`
`
`
`

`

`accelerated
`recovery
`performance
`
`451 CUff Road East, SUlle 106, Burnsville, MN 55337
`Phone: 952·808·0988 / Fax: 952·808·0980
`
`

`

`able
`
`ARP Manufacturing, llC
`
`the terminology
`
`the specifications
`
`the features & benefits
`
`the care, maintenance
`& technical support
`
`troubleshooting
`
`the warranty
`
`CONFIDENTIAL MATERIAL
`
`DO NOT DUPLICATE
`
`REV E 09/1 8/07
`
`

`

`ARP Operation Guide
`
`Introduction
`
`ARP is a new solution to old problems associated with
`traditional electrical
`therapeutic stimulation.
`ARP also
`presents new applications not previously addressed by
`traditional methods. ARP is a neuromuscular stimulator which
`introduces electrical signals to the body through conductive
`electrode pads to provide therapeutic treatment for a variety of
`conditions.
`
`WHAT MAKES ARP DIFFERENT?
`
`Traditionally. there have been two major methods in use for
`applying non-invasive electrical stimulation to the human body.
`The first method is to apply a single polarity, low frequency,
`alternating signal. The concept appears sound but runs into
`difficulty because the electrical resistance in the area of
`treatment may be relatively high at low frequencies. Oue to
`this high electrical resistance, the treatment can be quite
`uncomfortable for the patient. Using low frequency signals at
`the necessary high voltages, there is a loss in the intensity of
`the stimulation within the treatment area, limiting the value of
`the treatment The second method involves the interferential
`process. Interference current therapy consists of two (or more)
`medium frequency currents that are independent of each
`other. These medium frequency currents penetrate into the
`treatment area in order to interfere with each other and
`produce a low frequency. This low frequency produces a
`physiological response in tissue; however, with the production
`of this lower frequency also comes a loss of power. It has
`
`been expressed within the industry that power and frequency
`are the keys to effective electrical stimulation and therapy.
`
`ARP does not use either of the above techniques as its basis
`for action but has introduced a signal with simultaneous high
`and low freque ncies as a multi-phase signal with polarity. This
`produces a high power factor rather than just high voltages
`without producing discomfort to the patient. On the contrary. an
`almost immediate numbing occurs around the treatment area
`immediate,
`long
`lasting
`therapeutic response
`is
`and an
`obtained, often with as little as one treatment.
`
`DO YOU USE THE ARP TRAINER THE SAME WAY AS
`OTHER MACHINES?
`
`Basically no, while the operation and application through
`diagnostic placement of electrode pads is quite similar to other
`to the additional
`machines, ARP's differences are linked
`features of the machine. For example, there is a ~traveling"
`sensation of the stimulation that offers benefit to areas not
`being treated directly. This sensation is extremely useful in the
`treatment of migraine headaches. Also it is important for the
`therapist to understand the advanced penetration effects. The
`therapist must think on a multi-dimensional or, M3_0" level.
`Treatment extends beyond the surface area. Techniques for
`specific regions are discussed
`later in
`this manual with
`applications for specific conditions. Lastly, ARP is applied while
`the subject is put in motion. This is unique only to the ARP.
`
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`
`+1-1
`
`

`

`ARP Operation Guide
`
`WILL I NEED ADDITIONAL TRAINING?
`
`CAUTION :
`
`The ARP offers comprehensive lechnical support to present
`new and innovative treatment techniques for the therapist.
`
`TERMINOLOGY
`
`All special terms or terms with more than one common usage
`used in this manual are defined below. This definition as
`stated in this section represents the intended meaning of the
`term throughout this manual.
`
`• Continuous mode-Main Pulse stimulation is present at
`all times, DUTY CYCLE dial is at 20120.
`
`• Duty cycle -Variable amount of the time the main pulse
`is generated during a 20 second interval
`
`•
`
`•
`
`•
`
`Electrode pads -Pliable, conducting pads used to deliver
`electrical energy to the body areas being treated.
`
`Frequency -Number of main pulses per second.
`
`Intermittent mode - Method of operation when DUTY
`CYCLE dial is less than 20120.
`
`• Polarity -
`
`Indicates direction of electron flow.
`
`• Power - Effective stimulation intensity, which is
`determined by amplitude and frequency.
`
`the vasodilation effects of electromagnetic
`Because of
`stimulation, people wilh unknown conditions
`(epileptic,
`cardiac. cerebral, and vascular conditions, etc.) may
`experience untoward affects such as, dizziness, nausea,
`profuse perspiration, or fai nting. If this occurs, cease trealment
`immediately and recommend treatment by a physician to
`ascertain the ur)derlying cause(s) of said untoward affects.
`
`FEATURES & BENEFITS
`
`The ARP features a blend of two signals: a main pulse and a
`background signal. The unique signal provides a "3_0"
`stimulation of the body area being treated. Patient
`participation is another featUre of the treatment system,
`resulting in self-directed therapy. Additional detail of treatment
`techniques can be found in the ARP Guide. Electrostimulation
`therapy has been found to be beneficial for a variety of
`conditions:
`
`• Relaxation of muscle spasms
`•
`Prevention and retardation of disuse atrophy
`•
`Increase of local blood circulation
`• Muscle re-education
`•
`Immediate post-surgical stimulation of calf muscle to
`prevent v~nous thrombosis
`• Maintaining and increasing range of motion of body
`limbs
`
`SPECIFICATIONS
`
`Main Pulse Freque ncy - 40 to 500 pulses per second ; adjustable .
`Background Freque ncy -H igh frequency carrie r signal.
`O utput Power - Betwee n 0 a nd 3.5 watts.
`Polarity -Direction of electron fi ow is reversible.
`Battery -Lithium Io n Battery.
`External Power Supply -
`120/24 0 volts, 50/60 hertz input ; 12 volt DC output
`
`+ 1-2
`
`

`

`ARP Operation Guide
`
`In this chapter the following
`information will be discussed:
`
`• Description of Operator Controls
`• Accessories
`• Pad Placement Considerations
`• The Hunting Technique
`• Etectron Flow
`• Connecting the Cables
`• Pad Placement Techniques
`• How to Begin Treatment
`• Care, Maintenance & Technical Support
`• Troubleshooting
`• Warranty
`
`Polarity Switch
`
`Output Power Dial
`
`Power Switch
`
`Output
`
`Pulse Present
`
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`
`+ 2-1
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`

`

`ARP Operation Guide
`
`DESCRIPTION OF THE OPERATOR CONTROLS
`
`POWER SWITCH
`The on/off switch is a front panel rocker switch which connects
`(ON) and disconnects (OFF) the power produced by the power
`supply from the remainder of the circuit.
`
`PULSE PRESENT INDICATOR
`This small green light, located on the front panel, indicates the
`presence of the main pulse in the output signal. The
`brightness is relative to the strength of the main pulse signal:
`off when there is no main pulse, to full brightness at full main
`pulse power.
`
`OUTPUT POWER DIAL
`This dial controls the output power of the ARP . This control
`adjusts the power for any combination of electrode pads.
`Turning the dial in a clockwise direction increases the output
`power.
`
`70
`
`100
`
`_
`
`lUll Cre.e Maio PuIs
`•
`freQ (PPSJ
`
`lalla
`
`Pulse
`Present
`I SI:Zo
`
`+2-2
`
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`

`

`ARP Operation Guide
`
`BALANCE DIAL
`This dial is used to adjust the relative Power delivered to the
`electrode pad-pairs and balances power between three or
`more pads. When the dial is turned completely to either the
`right or left channel, power is absent in the oppos~e channel.
`
`POLARITY SWITCH
`This rocker switch, labeled NORM and REV, reverses the
`polarity of the output signal. When switching polarity, the
`output power will reduce to the "Orr level, then gradually
`increase back
`to
`the
`initial output
`level
`to avoid any
`unnecessary discomfort to the patient.
`In the "Normal"
`position the black pad is negative and the red pad is positive,
`conforming to normal electrical conventions.
`
`--/'-ARP Tip
`Before changing polarity, the power level should be low, yet
`perceptible by the patient.
`
`--/'- 2-3
`
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`
`

`

`ARP Operation Guide
`
`MAIN PULSE FREQUENCY CONTROL DIAL
`This dial is used to adjust the frequency of the main pulse.
`Rotating the control clockwise will increase the main pulse
`frequency.
`
`NOTE: PPS is an abbreviation for pulses per second .
`
`Increasing the frequency results in the patient feeling a
`deeper sensation with less muscle contraction.
`
`DUTY CYCLE DIAL
`The duty cycle period is equal to about 20 seconds. This dial
`is used to select the main pulse active duty cycle. When
`rotated completely clockwise, the main pulse output will be
`continuously present at the frequency selected. When the dial
`is rotated completely counter-clockwise, the main pulse output
`will be disabled. Any other duty cycle (ratio of main pulse
`present/absent) can be selected between these two limits.
`This is called the intermittent mode.
`
`10/20 Duty Cycle Setting
`
`Main Pulse
`Present
`
`Main Pulse
`Absent
`
`10 Seconds
`
`10 Seconds
`
`<1141---- 20 Seconds Total ___ .. ~
`
`+ARP Tip
`
`Use the Intermittent Mode when the therapist wishes to
`check on progress during
`the
`treatment
`time.
`The
`intermittent mode can be used to remove the stimulation for
`a period of time. During this lUll, the petient can be
`questioned about the feeling in the area being treated.
`
`+2-4
`
`CONFIDENTIAL MATERIAL DO NOT DUPLICATE
`
`

`

`ARP Operation Guide
`
`TIMER
`
`The operator selects the treatment time (in whole minutes)
`using the MINS button . Each time the MINS button is
`pressed, the timer count advances one minute. If the MINS
`button is held down, the timer will continue to advance.
`Pressing the START/STOP button will begin the countdown.
`When the timer counts down to zero, an audible tone is
`activated . The RESET button will allow the operator to reset
`the timer counter to zero and to turn off the audible tone.
`The timer is NOT a control feature.
`It does not turn the
`machine off; it is for monitoring the length of the treatment
`only.
`
`REAR PANEL CONTROLS
`
`ARP can be powered by either a Lithium Ion battery
`supplied by ARP Manufacturing only or an ARP external
`power supply. The POWER SOU RCE SELECTION switch
`should be pressed toward the female power jack AT ALL
`TIMES. If this switch is pushed in the opposite direction, the
`ARP will not turn on.
`
`TO USE BATIERY POWER:
`
`Attach the lithium ion battery to the back right side of the
`machine via the hook-loop attaching material (Le .. Velcro).
`Plug the battery into the female power jack. The door on the
`back of the machine is no longer used. This switch should
`be depressed towards the Jack for both battery and wall
`power supply sources.
`
`If external power is desired, unplug the battery and plug the
`external power supply connection into the Power Jack in the
`back panel and make sure
`the POWER SOURCE
`SELECTION switch is ALWAYS depressed toward the Jack.
`
`TO RECHARGE BATIERY:
`
`Remove the lithium ion battery from the back of the ARP
`unit and charge with approved lithium ion battery charger
`supplied by ARP manufacturing.
`
`See page 2-22 for battery care and placement
`instructions.
`
`Note:
`The entire ARP timer display begins to flash on and off when
`is
`low and
`the battery should be
`the battery voltage
`exchanged for a fully charged battery. If the patient is being
`treated at this pOint, finish the treatment and then complete
`the exchange.
`
`Notes on the AC Ad apter
`
`1. Your power supply operates on 10~V-240V AC 50/60HZ.
`2. Do not share the AC outlet with other power-consuming
`equipment such as a copy machine or shredder.
`3. Do not place any objects on the power cord or power unit.
`4. To disconnect the cord pull it out by the plug, never pull
`the cord itself.
`5. When the AC adapter is not used, unplug it from the AC
`outlet.
`6. Use only the AC adapter supplied. Do not use any other
`AC adapter.
`7. The AC adapter is for indoor use only and must be kept
`away from liquids.
`
`CONFIDENTIAL MATERIAL DO NOT DUPLICATE
`
`

`

`ARP Operation Guide
`
`SAFETY CIRCUITRY
`To prevent the delivery of sudden or unexpected power to a subject, protective circuitry
`and an audible alarm has been designed into the ARP unit.
`
`1.
`
`If the unit Is turned on with the OUTPUT POWER dial set above "1 " or, if the OUTPUT POWER dial is turned up too
`soon (1 second) after the POWER switch Is turned on, an alarm will sound and the output power will be disabled.
`
`To correct the problem:
`o turn the POWER switch off
`o resel the OUTPUT POWER dial to zero
`o turn the POWER SWITCH on
`
`proceed with the treatment
`
`2.
`
`If the BALANCE dial Is turned too quickly, an alarm may sound and the output power will be disabled.
`
`To correct the problem:
`
`o turn Ihe POWER switch off
`o reset the OUTPUT POWER dial to zero
`o tum the POWER SWITCH on
`
`proceed wrlh the treatment
`
`3.
`
`If a cable plug should disconnect from an electrode during treatment, an alarm may sound and the output power will
`be disabled.
`
`To correct the problem:
`
`o lurn the POWER switch off
`o reconnect the cable
`o reset the OUTPUT POWER dial to zero
`o turn the POWER SWITCH on
`
`proceed with the treatment
`
`CONFIDENTIAL MATERIAL DO NOT DUPLICATE
`
`

`

`ARP Operation Guide
`
`INDICATIONS
`
`ARP is Indicated for the following:
`Relaxation of muscle spasms
`Prevention or retardation of disuse atrophy
`Increasing local blood circulation
`Muscle fe-education
`Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis
`Maintaining or increasing range of motion
`
`CONTRAINDICATIONS
`
`ARP should not be used :
`On patients with implanted electrical devices
`Over known cancers
`On pregnant women
`
`WARNINGS
`
`Accelerated Recovery Performance makes the following warnings:
`Long term effects of chronic electrical stimulations are unknown.
`Adequate precautions should be taken in the case of persons with suspected or diagnosed heart problems.
`Adequate precautions should be taken in the case of persons with suspected or diagnosed
`epilepsy.
`DO NOT stimulate over the carotid sinus nerves, especially in patients with a known sensitivity to the carotid sinus reflex.
`Severe spasm of the laryngeal and pharyngeal muscles may occur when the electrodes are
`positioned over the neck or mouth. The contractions may be strong enough to close the airway or cause difficulty in breathing.
`ARP should NOT be applied transcerebrally (across the head).
`ARP should NOT be used over swollen, abraded, infected or inflamed areas or skin
`eruptions, e.g .. phlebitis, thrombophlebitis, or varicose veins.
`DO NOT use ARP with an external power source during storms.
`DO NOT use ARP in moving vehicles.
`Caution should be used in the transthoracic application in that introduction of electrical current
`into the heart may cause arrhythmias.
`ARP should be kept out of the reach of children.
`
`PRECAUTIONS
`
`Accelerated Recovery Performance further states that precautions should be observed in the presence of the following:
`1.
`wh en there is a tendency to hemorrhage following acute trauma or fracture,
`2.
`after recent surgical proced ures when muscle contractions may disrupt the healing process,
`3.
`over a menstruating uterus, or
`when sensory nerve damage is present by a loss of normal skin sensation.
`4.
`
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`
`+ 2-7
`
`

`

`ARP Operation Guide
`
`ElECTRON flOW
`
`If two pads are used, the
`Either two, three, or four electrode pads may be used to introduce the electrical signal to the subject.
`electrical signal is developed between the two electrodes. If four pads are used , the signal is developed across both pairs of pads
`as well as across the individual pads,
`If three pads are used, operation is similar to that using four pads, with one pad
`disconnected. A polarity reversal switch is provided to change the direction of the signal current at the pads.
`
`Black
`
`Red
`
`.~) O 2 Pads
`
`3 Pads
`
`Black o
`Red ~ ' \ i Red
`o
`0
`o
`0
`~JXt 4 Pads
`o
`0
`
`Black
`
`Black
`
`ARP's Signal Path , Normal Polarity
`
`+2-8
`
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`

`

`ARP Operation Guide
`
`CONNECTING THE CABLES
`
`When connecting the cables to the front panel, notice the
`OUTPUT plugs are colored. Notice that the blocks where the
`cable splits are colored the same color as the plug on that
`wire. Performance from each OUTPUT jack is identical.
`
`There are a variety of pad placement techniques used for
`specific conditions as discussed later in this chapter. Cable
`connections vary between the 2-pad placements and the 3-4
`pad placements. Please refer to the particular pad placement
`technique for further information on the cable connections to
`the front panel.
`
`CONFIDENTIAL MATERIAL DO NOT DUPLICATE
`
`-{'-
`
`2-9
`
`

`

`ARP Operation Guide
`
`PAD PlACEMENT TECHNIQUES
`
`SANDWICH FORMATION
`
`Note:
`Some people have occasionally experienced a slight -bump"
`if they are connected to the device while it is being turned on
`or off, even if the power dial is set at zero. To eliminate this
`situation, tum down the power dial as usual and disconnect
`the subject from ARP before turning off, or connect to the
`subject after it is turned on. If the subject already has pads
`applied prior to turning the device on, disconnect the pad
`cable(s) from the front panel, turn on, then reconnect the
`cable(s).
`
`CABLE CONNECTIONS
`Connect either cable into the left or right receptacle on the
`ARP front panel. Attach the red and black pads to the
`corresponding red and black leads.
`
`PATIENT PAD PLACEMENT
`Attach the pads to the affected area as illustrated. The
`electrons will flow from the black pad to the red pad with
`normal polarity selected. Reversing polarity will reverse the
`electron flow.
`
`+2-10
`
`CONFIDENTIAL MATERIAL DO NOT DUPLICATE
`
`

`

`ARP Operation Guide
`
`MODIFIED SANDWICH FORMATION
`
`CABLE CONNECTIONS
`Connect either cable into the left or right receptacle on the
`ARP front panel. Attach the red and black pads to the
`corresponding red and black leads.
`
`SUBJECT PAD PLACEMENT
`Attach the pads to the affected area as illustrated. The
`electrons will flow from the black pad to the red pad with
`normal polarity selected. Reversing polarity will reverse th e
`electron flow.
`
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`
`+ 2-11
`
`

`

`ARP Operation Guide
`
`LONGITUDINAL fORMATION
`
`CABLE CONNECTIONS
`Connect either cable into the left or right receptacle on the
`fronl panel. Attach the red and black pads to the
`ARP
`corresponding red and black leads.
`
`PATIENT PAD PLACEMENT
`Attach the pads to the affected area as illustrated . The
`electrons will flow from the black pad to the red pad with
`normal polarity selected. Reversing polarity will reverse the
`electron flow.
`
`+2-12
`
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`
`

`

`ARP Operation Guide
`
`T-FORMATION
`
`CABLE CONNECTIONS
`into the right or left
`Connect either of the colored cables
`receptacles on Ihe ARP fronl panel. On one of Ihe cables
`attach Ihe red and black pads 10 Ihe corresponding red and
`black leads. On Ihe olher cable attach Ihe red pad 10 Ihe
`corresponding
`red
`lead and
`take
`the unattached black
`connection and insert it in the hole in the cable junction. The
`eleclrons will flow from Ihe black pad 10 Ihe red pads wilh
`normal polarity selected. Reversing polarity will reverse the
`electron flow.
`
`SUBJECT PAD PLACEMENT
`Attach Ihe pads 10 Ihe affecled area as illuslraled. The
`eleclrons will flow from Ihe black pad 10 Ihe red pads with
`normal polarity selected. Reversing polarity will reverse the
`electron flow.
`
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`
`+2-13
`
`

`

`ARP Operation Guide
`
`BOX-FORMATION
`
`CABLE CONNECTIONS
`into the right or left
`Connect either of the colored cables
`output jacks on the ARP front panel. On each of the cables
`attach the red and black pads to the corresponding red and
`black leads.
`
`PATIENT PAD PLACEMENT
`Attach the pads to the affected area as illustrated. The
`electrons will flow from the black pad to the red pads with
`normal polarity selected. Reversing polarity will reverse the
`electron flow.
`
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`
`

`

`ARP Operation Guide
`
`ARP STERILIZATION PROCEDURES
`
`Sponge Conducting Pads
`
`The Sponge Conducting Pads are manufac1li!'d for the specific use with an electric modality such as the ARP. Other types of
`sponges will not provide equal conductivity over the treatment area . We highly recommend that each subject have their own set of
`sponges for sanitary reasons.
`If you are using the same sponges on several subjects, it is imperative that you sanitize these
`sponges between treatments. The sponges will become discolored and sometimes fray after several uses. This is the time to
`replace them and begin using new sponges. Use of typical sponge malerial could become harmful to the subjects. We recom(cid:173)
`mend using only the sponges manufactured for use with an electric modality.
`To sanitize the sponges follow the racommended procedure below:
`
`1. Use only antibacterial nontoxic+disinfectant solutions.
`
`2. Combine a solution of an antibacterial soap and very hot water to clean the sponges,
`squeezing them several times for sanitizing. Rinse the sponges completely
`in very hot water to release oils and dirt.
`
`In addition to sanitizing the sponges we recommend that you also use a disinfectant solution between treatments on the red and
`black electro conducting pads.
`
`DO NOT USE THE FOLLOWING :
`
`Alcohol, Ammonia. Bleach products or compounds, Iodine based solutions, i.e. Betadine/Povidone
`Iodine. and Quantinary Compounds, i.e. Zepharin Solution .
`
`Do not use any sanitizing devices such as steam or autoclave.
`
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`
`+2-15
`
`

`

`ARP Operation Guide
`
`CARE & MAINTENANCE
`
`• PREVENTATIVE MAINTENANCE
`Maintenance of ARP is simple but important. The ARP should at all times be free of dust and other foreign material and fluids. It
`should be stored in a dry environment. As with all electronic devices, observe caution when operating the ARP around fluids.
`
`• CLEANING THE ARP
`
`It is good practice to periodically clean the exterior surfaces of the ARP unit with a dry. or slightly damp cloth. 0 0 not immerse the
`unit.
`
`• BATTERY MAINTENANCE
`
`Store the battery in a cool, dry place and out of direct sunlight.
`DO NOT drop the battery or subject ~ to strong jolts.
`Always charge the battery soon after full use.
`DO NOT use another charger other than the Accelerated Recovery Performance Battery Charger.
`DO NOT use the battery for appliances other than specified .
`DO NOT use it below OC or above 40C (32F or 104F).
`DO NOT use an insuffiCiently charged or worn out battery.
`
`• CHARGING THE BATTERY
`
`1. Connect the AC Power Plug of the ARP Battery Charger to a 120 volt AC Outlet.
`2. Connect battery charger plug to battery.
`3. See instruction on charg er to determined when Batteries completely charged.
`
`NOTE: The useful operation time of the battery will gradually decrease after repeated use and recharging. The battery is no
`longer serviceable if the operation time is too short even after a sufficient charge.
`
`• EXCHANGING THE BATTERY
`
`When the battery needs exchanging (replacing), perform the following procedures:
`
`1. Unplug and remove the battery from back of ARP unit.
`2. Attach new/newly charged battery to back via hook-loop attaching material.
`3. Make sure power source selection switch is depressed toward the temale power plug.
`
`+2-16
`
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`

`

`ARP Operation Guide
`
`• TECHNICAL SUPPORT
`
`If you have any questions regarding the operation of ARP or advice on protocol techniques, please contact Accelerated Recovery
`Performance at 952-808-0988. We are always glad to hear from you and will try our best 10 assist in any way we can .
`
`SERVICE & PARTS
`
`• ORDERING PARTS
`
`To order parts and accessories for your unit, contact Accelerated Recovery Performance at 952-808-0988.
`Or visit us ARPwave.oom to order online.
`
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`
`+ 2·17
`
`

`

`ARP Troubleshooting Guide
`
`MAKE
`TURNED COMPLETELY TO 'ZERO', THEN
`TURN POWER SWITCH ON .
`
`I
`SUPPLY CONNECTIONS NOT
`SECURE. POSSIBLY POWER
`SUPPLY IS DEFECTIVE
`(RARE).
`
`I
`UNITTO
`POWER SUPPLY BOX, AND BOX TO POWER
`CORD .
`
`IF POWER SUPPLY DEEMED DEFECTIVE,
`RETURN TO MANUFACTURER FOR
`
`TO A WALL SWITCH THAT IS
`OFF
`
`ANOTHER OUTLET
`
`NO BATIERY ON UNIT (IF
`USING BATIERY POWER
`SOURCE)
`
`ATIACH BATIERY AND POSITION SWITCH
`IN BACK OF UNIT TOWARD THE FEMALE
`POWER PLUG.
`
`SET
`BY DEPRESSING TOWARD THE FEMALE
`POWER PLUG.
`
`INTERMITIMENT;
`PRESENT' INDICATOR LIGHT
`(GREEN) MAY OR MAY NOT
`CYCLE ON/OFF, DEPENDING ON
`CYCLE SETIING; TIMER DISPLAY
`
`I
`I
`PRESENT' INDICATOR
`(GREEN) IS OFF AND AN AUDIBLE
`TONE (BEEP) CAN BE HEARD
`
`I
`WAS NOT SET TO 'ZERO'
`PRIOR TO TURNING ON
`POWER SWITCH
`
`THE 'OUTPUT POWER' DIAL
`WAS TURNED UP TOO
`QUICKLY AFTER THE POWER
`SWITCH WAS TURNED ON
`
`THE 'BALANCE' DIAL WAS
`
`I
`CAUSED UNIT TO SHUT
`DOWN ... USUALLY IN A
`ROOM WITH FLOOR RUG
`
`TURN 'OUTPUT POWER' DIAL TO 'ZERO',
`TURN POWER SWITCH OFF THEN ON.
`WAIT 10 SECONDS; ADJUST 'BALANCE'
`DIAL; ADJUST 'OUTPUT POWER' DIAL
`SLOWLY.
`
`IN THE ROOM. RESET UNIT: TURN
`'OUTPUT POWER' DIAL TO 'ZERO', TURN
`POWER SWITCH OFF THEN ON . WAIT 10
`
`+ 2-18
`
`CONFIDENTIAL MATERIAL DO NOT DUPLICATE
`
`

`

`IRP Troubleshooting Guide
`
`IN PAD(S)
`
`A CABLE PIN IS
`DISCONNECTED FROM
`ONE OF THE PADS
`
`I
`TURN
`'ZERO', RECONNECT THE CABLE TO
`PAD, TURN POWER SWITCH OFF THEN
`ON. WAIT 10 SECONDS; ADJUST
`
`PATIENT NOT SENSITIVE
`TO THE MAIN PULSE
`NCY SELECTED
`uuc-nlNG
`
`TURN DOWN 'OUTPUT POWER',
`ADJUST FREQUENCY (LOWER),
`SLOWLY TURN
`'OUTPUT POWER'
`SEPARATE PADS
`
`PADS
`
`WALL PLUG-IN POWER
`SUPPLY CONNECTIONS
`NOT SECURE. POSSIBLY
`POWER SUPPLY IS
`DEFECTIVE (RARE).
`
`SECURE ALL CONNECTIONS: UNIT TO
`POWER SUPPLY BOX, AND BOX TO
`POWER CORD.
`
`IF POWER SUPPLY DEEMED
`DEFECTIVE, RETURN TO
`MANUFACTURER FOR REPLACEMENT.
`
`IN BACK OF UNIT IS SET
`INCORRECTLY.
`
`ING TOWARD FEMALE POWER JACK.
`
`CONFIDENTIAL MATERIAL DO NOT DUPLICATE
`
`+2-19
`
`

`

`ARP Troubleshooting Guide
`
`CHARGER AND THE RED LIGHT
`ON TOP IS OFF
`
`INTO WALL
`
`NO POWER A THE WALL
`OUTLET
`
`CHANGE AC POWER SOURCE
`
`+2-20
`
`CONFIDENTIAL MATERIAL DO NOT DUPLICATE
`
`

`

`ARP Operation Guide
`
`Accelerated Recovery Performance warrants that ARP is free from defects in material and workmanship.
`
`This warranty period is two (2) years from the date of delivery to the original purchaser and is owner-specific. The fi rst year of the
`warranty covers parts and labor while the second year of the warranty covers parts only. Repair or replacement will be made in a
`timely manner of receipt of the defective unit.
`
`WARRANTY INFORMATION
`
`This warranty does NOT cover:
`1)
`Replacement parts or labor furnished by anyone other than Accelerated Recovery
`Performance:
`2)
`Defecls or damage caused by labor furnished by anyone other than Accelerated Recovery
`Performance or its appointed agents;
`3)
`Deliberate and/or intentional damage;
`4)
`Damage inflicted as a result of an act of God;
`Damage caused by unreasonable use;
`5)
`6)
`Damage caused by lack of necessary maintenance;
`7)
`Accessories such as cables, pads, sponges, straps, power supply. charger and battery;
`8)
`Damage caused by operator error or lack of proper training in the use of the equipment;
`9)
`Damage inflicted as a result of criminal action.
`
`Accelerated Recovery Performance shall not be liable for incidental or consequential damages to property or business except in
`those states where this exclusion is eXRressly disallowed .
`
`To file a claim under this warrantyl the owner must:
`Put the nature of the complaint in writing and submit to Accelerated Recovery Performance by
`FAX at (952) 808-0986 or mail to 451 Cliff Road East, Suite 106, Burnsville, MN 55337.
`
`Accelerated Recovery Performance does not authorize any person, agent or representative to create any additional or other
`obligation or liability in connection with the sale or use of ARP. Any such representation, granting or agreement shall be null and
`void and shall have no effect whatsoever.
`
`12376 River Ridge Circle, Burnsville, MN 55337
`Phone: 952-808-0988
`Fax: 952-808-0986
`ARPprogram.com
`
`ARP Marwfac:luring, LLC
`
`CONFIDENTIAL MATERIAL DO NOT DUPLICATE
`
`+ 2-21
`
`

`

`ARP Operation Guide
`
`Banerv Placement Instrucdon
`
`The ARP battery charger is programmed to charge 4 hours.
`However. if the battery is needed sooner. it may be removed
`from the charger after 2 1/2 hours for a nearly full charge.
`
`The charger light glows red at beginning of charging cycle.
`turns to orange as the lithium ion battery is going thru
`charging, and finally turns green after 4 hours (the cycle
`ends).
`
`Do not attempt to charge the lithium ion battery with any other
`charger.
`
`Unlike the previous lead-acid battery. this battery may be
`allowed to completely discharge without harm. When the
`battery comes to the end of its current discharge cycle, the
`ARP will cease to operate. At this point, recharge the battery
`with the ARP battery charger and if further ARP operation is
`desired, plug the ARP into the power supply.
`
`These lithium ion batteries have an average number of
`recycles of 500. Depending upon the frequency of use, these
`batteries may tast up to three years or longer.
`
`SEE BA TIERY FOR ADDITIONAL CAUTIONS
`
`Position plug into receptacle.
`
`Position battery as shown and press in
`against machine to permanently place
`battery via hook and loop (Velcro).
`
`+2-22
`
`CONFIDENTIAL MATERIAL DO NOT DUPLICATE
`
`