Cardiovention, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiovention, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cardiovention, Inc. has 4 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Historical record: 4 cleared submissions from 2002 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiovention, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiovention, Inc.
4 devices
Cleared
Aug 22, 2003
CARDIOVENTION CORX IOS-200 SYSTEM, MODEL IOS-200
Cardiovascular
50d
Cleared
Feb 26, 2003
MODIFICATION TO CARDIOVENTION POWERBASE CONSOLE, MODEL PCB-100
Cardiovascular
42d
Cleared
Jan 08, 2003
CARDIOVENTION POWERBASE CONSOLE, MODEL PBC-100
Cardiovascular
231d
Cleared
Apr 09, 2002
CARDIOVENTION CORX SYSTEM, MODEL FG 0001
Cardiovascular
260d