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