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U.S. Department of Health and Human Services

510(k) Premarket Notification

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ProductCode: FTL Applicant: ATRIUM MEDICAL CORPORATION Decision Date To: 11/21/2019
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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
atrium centrilfx mesh ATRIUM MEDICAL CORPORATION K110110 02/15/2011
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