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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 14 Results
ProductCode: FTL Applicant: ATRIUM MEDICAL CORP Decision Date To: 10/23/2019
 
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c-qur, c-qur fx, c-qur tacshield, c-qur v-patch, c-qur centrifx, c-qur mosaic ATRIUM MEDICAL CORPORATION K151386 10/22/2015
prolite mesh, prolite ultra mesh, proloop mesh plug ATRIUM MEDICAL CORPORATION K151437 08/27/2015
c-qur rpm mesh ATRIUM MEDICAL CORP. K121070 04/26/2012
atrium centrilfx mesh ATRIUM MEDICAL CORPORATION K110110 02/15/2011
atrium c-qur ovt mesh ATRIUM MEDICAL CORP. K100076 01/26/2010
c-qur v -patch mesh ATRIUM MEDICAL CORP. K090909 06/04/2009
atrium prolite s mesh ATRIUM MEDICAL CORP. K082748 01/14/2009
c-qur edge mesh v-patch ATRIUM MEDICAL CORP. K080691 04/16/2008
c-qur lite mesh v-patch ATRIUM MEDICAL CORP. K080688 04/16/2008
atrium prolite ultra s mesh ATRIUM MEDICAL CORP. K070192 03/08/2007
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