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U.S. Department of Health and Human Services

510(k) Premarket Notification
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31 to 40 of 68 Results
ProductCode: FPA Applicant: BAXTER HEALTHCARE CORP Decision Date To: 01/21/2017
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510(K)
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continuflo solution set/secondary medication set BAXTER HEALTHCARE CORP. K961225 06/21/1996
control-a-flo(tm) regulator BAXTER HEALTHCARE CORP. K940867 05/05/1994
dual luer lock cap BAXTER HEALTHCARE CORP. K981318 04/22/1998
dual luer lock cap, model 2c6250 BAXTER HEALTHCARE CORP. K101385 06/22/2010
extended life injection site BAXTER HEALTHCARE CORP. K882007 06/20/1988
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
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