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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: 12/07/2016
 
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volumetric pump solution set w/integral airway BAXTER HEALTHCARE CORP. K893646 12/06/1989
volumetric pump solution set modified cassette BAXTER HEALTHCARE CORP. K912141 09/11/1991
volumetric pump solution set for flo-gard 8000 BAXTER HEALTHCARE CORP. K893716 09/18/1989
v-link antimicrobial luer activated device and extension sets with v-link antimicrobial luer activated device BAXTER HEALTHCARE CORP. K081289 08/04/2008
sub-q-set(r) subcutaneous infusion set BAXTER HEALTHCARE CORP. K925362 08/28/1993
solution set/extension set BAXTER HEALTHCARE CORPORATION K142011 08/18/2014
solution set with 1.2 micron air eliminating filter BAXTER HEALTHCARE CORP. K952074 07/27/1995
solution set with 1.2 micron air eliminating filter Baxter Healthcare Corporation K161808 06/21/2017
solution set for epidural use BAXTER HEALTHCARE CORPORATION K161323 11/30/2016
solution administration with luer access injection site BAXTER HEALTHCARE CORP. K042936 11/26/2004
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