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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: 12/07/2016
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neutral luer activated device and extension sets with neutral luer activated device BAXTER HEALTHCARE CORPORATION - RENAL DIVISION K120443 05/22/2012
neutral luer activated device (one-link needle-free iv connector) and extension sets BAXTER HEALTHCARE CORP. K132734 10/08/2013
needle*lock(tm) with interlink(tm) injection site BAXTER HEALTHCARE CORP. K914048 11/27/1991
luer access injection site BAXTER HEALTHCARE CORP. K984060 07/26/1999
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
iv fat emulsion administration sets Baxter Healthcare Corporation K172544 09/22/2017
intravascular extension sets and accessories Baxter Healthcare Corporation K192366 07/20/2020
intravascular extension set Baxter Healthcare Corporation K210430 06/18/2021
intravascular administration sets Baxter Healthcare Corporation K203609 09/30/2021
interlink(tm) injection site BAXTER HEALTHCARE CORP. K922558 10/19/1992
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