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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 30 Results
ProductCode: FPA Applicant: ABBOTT LABORATORIES Decision Date To: 10/23/2014
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510(K)
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iv extension set sl ABBOTT LABORATORIES K791930 10/26/1979
venoset dual-rate piggyback w/ivex & ABBOTT LABORATORIES K821578 06/22/1982
vented nitroglycerin i.v. set ABBOTT LABORATORIES K821515 06/09/1982
provider pump set w/infusion cartridge ABBOTT LABORATORIES K934513 07/29/1994
lifeshield additive piercing pin ABBOTT LABORATORIES K002006 08/10/2000
venipuncture valve ABBOTT LABORATORIES K832123 08/12/1983
venovalve(tm) ABBOTT LABORATORIES K881234 06/13/1988
iv set that reverts to kvo rate ABBOTT LABORATORIES K770744 05/26/1977
lifeshield anesthesia set ABBOTT LABORATORIES K913982 11/05/1992
energized drug container system ABBOTT LABORATORIES K934119 06/09/1994
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