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.
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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