Ex Parte RobertsDownload PDFPatent Trial and Appeal BoardMar 17, 201612189624 (P.T.A.B. Mar. 17, 2016) Copy Citation UNITED STA TES p A TENT AND TRADEMARK OFFICE APPLICATION NO. FILING DATE 12/189,624 08/1112008 28075 7590 03/21/2016 SEAGER, TUFTE & WICKHEM, LLP 100 SOUTH 5TH STREET SUITE 600 MINNEAPOLIS, MN 55402 FIRST NAMED INVENTOR Nick Roberts UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O. Box 1450 Alexandria, Virginia 22313-1450 www .uspto.gov ATTORNEY DOCKET NO. CONFIRMATION NO. SMASD-14US 7360 EXAMINER REYES, REGINALD R ART UNIT PAPER NUMBER 3686 NOTIFICATION DATE DELIVERY MODE 03/21/2016 ELECTRONIC Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. Notice of the Office communication was sent electronically on above-indicated "Notification Date" to the following e-mail address( es): GEN.USPTO@stwiplaw.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte NICK ROBERTS Appeal2013-008210 Application 12/189,6241 Technology Center 3600 Before HUBERT C. LORIN, BIBHU R. MOHANTY, and BRADLEY B. BAY AT, Administrative Patent Judges. LORIN, Administrative Patent Judge. DECISION ON APPEAL STATEMENT OF THE CASE Nick Roberts (Appellant) seeks our review under 35 U.S.C. § 134 of the Examiner's Final rejection of claims 1--4, 7, 13-16, 19, 26, 27, and 29- 51. We have jurisdiction under 35 U.S.C. § 6(b) (2002). SUMMARY OF DECISION We REVERSE. 1 The Appellant identifies Smiths Medical ASD, Inc., as the real party in interest. App. Br. 3. Appeal2013-008210 Application 12/189,624 THE INVENTION Claim 1, reproduced below, is illustrative of the subject matter on appeal. 1. A method of tracking changed parameters in a plurality of medical infusion pumps, each of the medical infusion pumps having first, common metadata associated therewith by which to communicate a defined device identifier for that medical infusion pump and second metadata associated therewith by which to communicate operational data collected by that medical infusion pump, the method comprising: programming each medical device to have the first common metadata and the respective second metadata; establishing communication sessions between the medical infusion pumps and a medical device server; in respect of each of the medical infusion pumps, communicating a packet of information including the first metadata and defined device identifier for that medical infusion pump and the second metadata and an original parameter value of operational data, an updated parameter value of operational data, and a final parameter value of operational data from that medical infusion pump to the medical device server; processing each packet of information to determine the defined device identifier communicated with the first metadata; and storing the original parameter value, the updated parameter value, and the final parameter value of the operational data in relation to the second metadata of each respective medical infusion pump on the medical device server for the respective medical infusion pump in relation to the defined device identifier of the first metadata of that medical infusion pump. 2 Appeal2013-008210 Application 12/189,624 THE REJECTIONS The Examiner relies upon the following as evidence of unpatentability: Samuels son Lee Leibner-Druska Ryu US 2004/0073276 Al US 2005/0144204 Al US 2006/0100746 Al US 2006/0248465 Al The following rejections are before us for review: Apr. 15, 2004 June 30, 2005 May 11, 2006 Nov. 2, 2006 1. Claims 1--4, 7, 13-16, and 19 are rejected under 35 U.S.C. §103(a) as being unpatentable over Leibner-Druska, Lee, and Samuelsson. 2. Claims 26, 27, 30--40, 42-51 are rejected under 35 U.S.C. §103(a) as being unpatentable over Leibner-Druska and Samuelsson. 3. Claims 29 and 41 are rejected under 35 U.S.C. §103(a) as being unpatentable over Leibner-Druska, Samuelsson, and Ryu. ISSUES Did the Examiner err in rejecting claims 1--4, 7, 13-16, and 19 under 35 U.S.C. §103(a) as being unpatentable over Leibner-Druska, Lee, and Samuelsson; claims 26, 27, 30--40, 42-51under35 U.S.C. §103(a) as being unpatentable over Leibner-Druska and Samuelsson; and claims 29 and 41 under 35 U.S.C. § 103(a) as being unpatentable over Leibner-Druska, Samuelsson, and Ryu? 3 Appeal2013-008210 Application 12/189,624 ANALYSIS The rejection of claims 1--4, 7, 13-16, and 19 under 35 U.S.C. §103(a) as being unpatentable over Leibner-Druska, Lee, and Samuelsson. Independent claim 1 includes the limitation: each of the medical infusion pumps having first, common metadata associated therewith by which to communicate a defined device identifier for that medical infusion pump and second metadata associated therewith by which to communicate operational data collected by that medical infusion pump. The Examiner found said claim limitation disclosed in paragraphs 16 and 20 of Leibner-Druska. See Final Act. 3; see also Ans. 5---6. According to the Examiner: Examiner broadly interprets metadata as data about data. So in paragraph 20 of Leibner-Druska teaches pumping parameter for infusing the medical fluid to the patient (first metadata) and comparing the uploaded pumping parameter to a data base of predetermined pumping parameter limits and providing an alert if the uploaded pumping parameter is outside the limits (second metadata). Ans. 5---6. We make the following observation. Appellant contends that the cited prior art fails to disclose tagging via metadata (see, e.g., "tagging to communicate" (Br. 24)). According to Appellant, "[e]ach medical device must send its device identifier tagged by metadata that defines it as device identifier data. As a consequence, each of the medical devices has common, first metadata being the tag for the device identifier data." Br. 19. However, the claims do not require metadata tags or tagging. The claimed subject matter provides for, more broadly, metadata which "[is] associated [with a medical infusion pump] by which to communicate a defined device identifier for that medical infusion pump" (claim 1 ). 4 Appeal2013-008210 Application 12/189,624 Notwithstanding that the Appellant's argument as to tagging is not commensurate in scope with what is claimed, we will not sustain the Examiner's rejection. Paragraph 20 of Leibner-Dmska teaches communicating and displaying a "pumping parameter, and associated identification of the infusion pump" on a monitor. Thus, paragraph 20 discloses a device identifier for a medical infusion pump, and operational data collected by that medical infusion pump. However, the cited passage provides no indication that the pumping parameter, which the Examiner found corresponds to "first, common metadata," is used "to communicate a defined device identifier" as required by claim 1. Nor does the cited passage provide any indication that the predetermined pumping parameter limits, which the Examiner found correspond to "second metadata," are used "to communicate operational data" as claimed. For the foregoing reasons, a prim a facie case of obviousness has not been made out in the first instance by a preponderance of the evidence. Accordingly, the rejection of independent claim 1, and claims 2--4, and 7 which depend from it, is not sustained. Independent claim 13 recites a similar limitation, and the Examiner's rejection suffers from the same deficiency as the rejection of independent claim 1. See Final Act. 3. Accordingly, the rejection of independent claim 13, and claims 14--16, and 19 which depend from it, is not sustained. 5 Appeal2013-008210 Application 12/189,624 The rejection of claims 26, 27, 30--40, 42-51 under 35 U.S.C. §103(a) as being unpatentable over Leibner-Druska and Samuelsson. Independent claims 26, 38, 39, and 51 recite a similar limitation, and the Examiner's rejection suffers from the same deficiency as the rejection of independent claim 1. See Final Act. 6-7;see also Ans. 6-8. Accordingly, the rejection of independent claims 26, 38, 39, and 51, and claims 27, 30-37, 40, and 42-50 which depend from them, are not sustained for similar reasons. The rejection of claims 29 and 41under35 U.S.C. §103(a) as being unpatentable over Leibner-Druska, Samuelsson, and Ryu These rejections are directed to claims which depend from independent claims 26 and 39, whose rejections we have not sustained, as described above. For the same reasons, we will not sustain the rejections of claims 29 and 41 over the cited prior art. Cf In re Fritch, 972 F.2d 1260, 1266 (Fed. Cir. 1992) ("[D]ependent claims are nonobvious if the independent claims from which they depend are nonobvious. "). CONCLUSIONS The rejections of claims 1--4, 7, 13-16, and 19 under 35 U.S.C. § 103(a) as being unpatentable over Leibner-Druska, Lee, and Samuelsson; claims 26, 27, 30--40, 42-51under35U.S.C.§103(a) as being unpatentable over Leibner-Druska and Samuelsson; and claims 29 and 41under35 U.S.C. § 103(a) as being unpatentable over Leibner-Druska, Samuelsson, and Ryu are not sustained. 6 Appeal2013-008210 Application 12/189,624 DECISION The decision of the Examiner to reject claims 1--4, 7, 13-16, 19, 26, 27, and 29-51 is reversed. REVERSED 7 Copy with citationCopy as parenthetical citation