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U.S. Department of Health and Human Services

510(K) Premarket Notification
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261 to 270 of 500 Results *
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Device Name
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Applicant
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510(K)
Number
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Decision
Date
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sensititre 18-24 hours susceptibility plates TREK DIAGNOSTIC SYSTEMS, INC. k001573 07/18/2000
s.m.a.r.t. nitinol stent transhepatic biliary system CORDIS CORP. k001843 07/18/2000
modification to centaur spinal system HOWMEDICA OSTEONICS CORP. k001844 07/19/2000
microvasive lithotriptor flexprobe ii BOSTON SCIENTIFIC CORP. k002084 07/19/2000
pta balloon catheter COOK, INC. k001087 07/20/2000
dr180-ii NORTHEAST MONITORING, INC. k001288 07/20/2000
stethos, model stxxyyzz or 001 xxx, stethos link, model slxxyyzz or 002 xxx ANDROMED, INC. k001306 07/20/2000
cpap system, model 102001 SIMS PORTEX, INC. k001318 07/20/2000
calciject CENTRIX, INC. k001050 07/21/2000
aria DEL MAR MEDICAL SYSTEMS, LLC. k001317 07/21/2000

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
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