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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 3 of 3 Results
ProductCode: FPA Applicant: BAXTER HEALTHCARE CORPORATION Decision Date To: 07/22/2014
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interlink system extension set with cont baxter healthcare corporation K121634 06/29/2012
neutral luer activated device and extens baxter healthcare corporation - renal di K120443 05/22/2012
clearlink luer activated valve, clearlin baxter healthcare corporation K112893 10/18/2011
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