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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 30 Results
ProductCode: FPA Applicant: ABBOTT LABORATORIES Decision Date To: 10/26/2016
 
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510(K)
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energized container system ABBOTT LABORATORIES K925418 11/03/1993
energized container system (modification) ABBOTT LABORATORIES K954283 05/29/1996
energized drug container system ABBOTT LABORATORIES K934119 06/09/1994
i.v. pump set for fat emulsion ABBOTT LABORATORIES K771593 09/12/1977
in-line burette set ABBOTT LABORATORIES K772036 11/16/1977
iv extension set sl ABBOTT LABORATORIES K791930 10/26/1979
iv set that reverts to kvo rate ABBOTT LABORATORIES K770744 05/26/1977
lifecare plumset vented secondary i.v. set ABBOTT LABORATORIES K933326 03/28/1994
lifeshield additive piercing pin ABBOTT LABORATORIES K002006 08/10/2000
lifeshield anesthesia set ABBOTT LABORATORIES K913982 11/05/1992
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