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U.S. Department of Health and Human Services

510(k) Premarket Notification
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51 to 60 of 68 Results
ProductCode: FPA Applicant: BAXTER HEALTHCARE CORP Decision Date To: 09/26/2016
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interlink(tm) injection site BAXTER HEALTHCARE CORP. K925126 06/18/1993
large bore stopcock with rotating male luer lock/large bore stopcock with extension set, gang large bore stopcock manifo BAXTER HEALTHCARE CORP. K130245 03/01/2013
luer access injection site BAXTER HEALTHCARE CORP. K984060 07/26/1999
needle*lock(tm) with interlink(tm) injection site BAXTER HEALTHCARE CORP. K914048 11/27/1991
neutral luer activated device (one-link needle-free iv connector) and extension sets BAXTER HEALTHCARE CORP. K132734 10/08/2013
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
solution administration set BAXTER HEALTHCARE CORP. K981792 08/17/1998
solution administration set with 0.22 micron high pressure extended life filter BAXTER HEALTHCARE CORP. K964850 02/25/1997
solution administration set with capped luer activated valve BAXTER HEALTHCARE CORP. K974571 05/21/1998
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