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`IN THE UNITED STATES PATENT AND TRADEMARK OFFICE
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`
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`In re Inter Partes Review of:
`U.S. Patent No. 8,776,794
`Issued: July 15, 2014
`Application No.: 14/065,951
`U.S. Filing Date: Oct. 29, 2013
`
`For: Nitric Oxide Delivery Device
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`FILED VIA PRPS
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`SUPPLEMENTAL DECLARATION OF WARREN P. HEIM, P.E.
`IN SUPPORT OF PATENT OWNER’S RESPONSE TO
`PETITION FOR INTER PARTES REVIEW
`OF U.S. PATENT NO. 8,776,794
`
`
`
`
`
`Ex. 2042-0001
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`
`
`Supplemental Declaration of Warren P. Heim, P.E. in Support of Patent Owner’s
`Response to Petition for Inter Partes Review of U.S. Patent No. 8,776,794
`
`
`I, Warren P. Heim, P.E. resident of Boulder, Colorado, hereby declare as
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`follows:
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`1.
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`I hereby declare that Exhibit 2027 is a true and correct copy of a brochure I
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`obtained at http://micromedical.co.uk/downloads/manuals/Printernox2.pdf
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`(last visited on December 30, 2015) relating to the CareFusion PrinterNOx
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`device. The site http://micromedical.co.uk/ automatically redirects to the
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`main CareFusion website.
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`2.
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`I hereby declare that Exhibit 2036 is a true and correct copy of a document I
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`obtained
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`at
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`https://www.maximintegrated.com/en/products/ibutton/products/1wire_adap
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`ters.cfm (last visited on December 30, 2015) relating to 1-Wire Adapters.
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`3.
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`I hereby declare that Exhibit 2037 is a true and correct copy of a document I
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`obtained at https://www.maximintegrated.com/en/products/digital/memory-
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`products/DS1996.html (last visited on December 30, 2015) relating to the
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`Maxim DS1996 product.
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`4.
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`I hereby declare that Exhibit 2039 is a true and correct copy of a document I
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`obtained
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`at
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`http://www.fda.gov/medicaldevices/deviceregulationandguidance/databases/
`
`default.htm (last visited on December 30, 2015) listing FDA medical device
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`databases.
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`
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`
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`1
`
`Ex. 2042-0002
`
`
`
`Supplemental Declaration of Warren P. Heim, P.E. in Support of Patent Owner's
`Response to Petition for Inter Partes Review of U.S. Patent No. 8,776,794
`
`5.
`
`I hereby declare that Exhibit 2040 is a true and correct copy of a document I
`
`obtained
`
`at
`
`http://www. fda.gov I down I oads/medicaldevices/ deviceregulationandguidanc
`
`e/guidancedocuments/ucm284443.pdf (last visited on December 30, 2015)
`
`relating to FDA's 510(k) program.
`
`6.
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`In signing this declaration, I recognize that the declaration will be filed as
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`evidence in a contested proceeding before the Patent Trial and Appeal Board
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`of the United States Patent and Trademark Office. If cross-examination is
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`required of me, I will appear for cross-examination within the United States
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`during the time allotted for cross-examination.
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`7.
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`I hereby declare that all statements made herein of my own knowledge are
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`true and that all statements made on information and belief are believed to
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`be true; and further that these statement were made with the knowledge that
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`willful false statements and the like so made are punishable by fine or
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`imprisonment, or both, under Section 1001 of Title 18 of the United States
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`Code and that such willful false statement may jeopardize the validity of the
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`application or any patent issued thereon.
`
`Warren P. Heim, P .E.
`
`Date
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`2
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`Ex. 2042-0003
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