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U.S. Department of Health and Human Services

510(k) Premarket Notification
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41 to 50 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 04/02/2015
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510(K)
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model number: rms1-2604, rms1-2614, rms1-2404, rms1-2414, rms2-2604, rms2-2614, rms2-2404, rms2-2414, rms3-2604, rms3-26 REPRO-MED SYSTEMS, INC. DBA RMS MEDICAL PRODUCTS K122404 05/06/2013
orbit infusion set YPSOMED AG K130468 03/19/2013
kdl disposable infusion set SHANGHAI KINDLY ENT. DEVELOPMENT GROUP CO., LTD. K112204 09/10/2012
zyno medical administration set ZYNO MEDICAL LLC K120685 09/07/2012
arisure neutral valve YUKON MEDICAL, LLC K120799 03/30/2012
rms subcutaneous needle set REPRO-MED SYSTEMS, INC. K102512 05/20/2011
in vision-plus nano with neutral advantage technology RYMED TECHNOLOGIES, INC. K093489 07/29/2010
autostart burette ANALYTICA PTY LTD K092905 03/04/2010
disposable tpe infusion set SHAN DONG WEI GAO GROUP MEDICAL POLYMER PRODUCTS K090459 10/13/2009
disposable infusion set SHAN DONG WEI GAO GROUP MEDICAL POLYMER PRODUCTS K090012 06/11/2009
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