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FDA 510(k) Applications Submitted by ATRIUM MEDICAL CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130142
01/22/2013
FLIXENE IFG VASCULAR GRAFT
ATRIUM MEDICAL CORPORATION
K110110
01/14/2011
ATRIUM CENTRILFX MESH
ATRIUM MEDICAL CORPORATION
K201305
05/15/2020
Auto transfusion (ATS) Chest Drains: Ocean Water Seal Chest Drain, Oasis Dry Suction Water Seal Chest Drain, Express Dry Seal Chest Drain
Atrium Medical Corporation
K151386
05/26/2015
C-QUR, C-QUR FX, C-QUR TacShield, C-QUR V-Patch, C-QUR CentriFX, C-QUR Mosaic
ATRIUM MEDICAL CORPORATION
K151437
05/29/2015
ProLite Mesh, ProLite Ultra Mesh, ProLoop Mesh Plug
ATRIUM MEDICAL CORPORATION
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