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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 68 Results
ProductCode: FPA Applicant: BAXTER HEALTHCARE CORP Decision Date To: 10/22/2016
 
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510(K)
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auto-syringe infusion set BAXTER HEALTHCARE CORP. K781036 08/10/1978
auto-syringe micro volume extension set BAXTER HEALTHCARE CORP. K811463 06/12/1981
auto-syringe sub-cuteaneous set BAXTER HEALTHCARE CORP. K813194 12/02/1981
blood/solution set w/pressure pump BAXTER HEALTHCARE CORP. K881321 06/16/1988
check valve BAXTER HEALTHCARE CORP. K881052 05/26/1988
extended life injection site BAXTER HEALTHCARE CORP. K882007 06/20/1988
safesite injection site and blunt cannula BAXTER HEALTHCARE CORP. K883638 09/23/1988
secondary solution administration set w/sheath BAXTER HEALTHCARE CORP. K880482 03/18/1988
extension set w/flow regulator BAXTER HEALTHCARE CORP. K890489 06/08/1989
volumetric pump solution set for flo-gard 8000 BAXTER HEALTHCARE CORP. K893716 09/18/1989
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