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U.S. Department of Health and Human Services

510(k) Premarket Notification
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21 to 30 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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extension set w/flow regulator BAXTER HEALTHCARE CORP. K890489 06/08/1989
fenwal(r) 40/150 micron dual screen filter BAXTER HEALTHCARE CORP. K932301 11/10/1993
flowease [subcutaneous] infusion set BAXTER HEALTHCARE CORP. K121092 06/29/2012
huber needle extension set with standard y-injection site, interlink y-injection site, interlink t-injection site BAXTER HEALTHCARE CORP. K961495 06/26/1996
in-line vial connection site BAXTER HEALTHCARE CORP. K900909 05/18/1990
injection site with luer lock BAXTER HEALTHCARE CORP. K915828 05/15/1992
interlink adapter for conventional y-site BAXTER HEALTHCARE CORP. K962893 10/18/1996
interlink micro-infusion manifold extension sets BAXTER HEALTHCARE CORP. K970438 04/02/1997
interlink s / clearlink system / v-link lad with vitalshield protective coating non-dehp catheter extension set kits, BAXTER HEALTHCARE CORP. K103551 03/25/2011
interlink system - t-connector extension set BAXTER HEALTHCARE CORP. K921899 04/20/1993
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