Jomed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jomed, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Jomed, Inc. has 6 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 6 cleared submissions from 2001 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Jomed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jomed, Inc.
6 devices
Cleared
Jun 23, 2003
JOVUS EAGLE EYE F/X 2.9F IVUS CATHETER, MODEL 85900
Cardiovascular
55d
Cleared
May 28, 2003
IN-VISION IMAGING SYSTEM
Cardiovascular
48d
Cleared
May 14, 2003
JOWIRE ASAHI PTCA CATHETER GUIDE WIRES, MODELS...
Cardiovascular
22d
Cleared
Dec 16, 2002
JOWIRE NEO'S PTCA CATHETER GUIDEWIRES, MODELS AG141000, AG142000, AG143000,...
Cardiovascular
118d
Cleared
May 17, 2002
SMARTWIRE/SMARTMAP PRESSURE SYSTEM
Cardiovascular
30d
Cleared
Jan 18, 2001
TRAK BACK II
Cardiovascular
29d