Atrium Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Atrium Medical Corp. - FDA 510(k) Cleared Devices
63
Total
61
Cleared
0
Denied
Atrium Medical Corp. has 61 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 61 cleared submissions from 1981 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Atrium Medical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Atrium Medical Corp.
63 devices
Cleared
Feb 28, 2013
EDRAIN CHEST DRAINAGE SYSTEM
General & Plastic Surgery
41d
Cleared
Aug 17, 2012
ATRIUM FLIXENE IFG VASCULAR GRAFT
Cardiovascular
29d
Cleared
Apr 26, 2012
C-QUR RPM MESH
General & Plastic Surgery
17d
Cleared
Nov 17, 2011
CLEARWAY RX NB CATHETER
Cardiovascular
28d
Cleared
Oct 05, 2010
ATRIUM GRADUATED WALL FLIXENE AX-BIFEM GRAFT
Cardiovascular
26d
Cleared
Apr 20, 2010
CLEARWAY OTW MODEL 85912
Cardiovascular
167d
Cleared
Jan 26, 2010
ATRIUM C-QUR OVT MESH
General & Plastic Surgery
14d
Cleared
Jun 04, 2009
C-QUR V -PATCH MESH
General & Plastic Surgery
64d
Cleared
Jan 14, 2009
ATRIUM PROLITE S MESH
General & Plastic Surgery
117d
Cleared
Jul 25, 2008
EXPRESS CHEST DRAIN
General Hospital
37d
Cleared
Apr 16, 2008
C-QUR LITE MESH V-PATCH
General & Plastic Surgery
36d
Cleared
Apr 16, 2008
C-QUR EDGE MESH V-PATCH
General & Plastic Surgery
36d
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