Cardiovention, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cardiovention, Inc. Cardiovascular ✕
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