Cardiovention, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K032068CARDIOVENTION CORX IOS-200 SYSTEM, MODEL IOS-200August 22, 2003
K030141MODIFICATION TO CARDIOVENTION POWERBASE CONSOLE, MODEL PCB-100February 26, 2003
K021694CARDIOVENTION POWERBASE CONSOLE, MODEL PBC-100January 8, 2003
K012325CARDIOVENTION CORX SYSTEM, MODEL FG 0001April 9, 2002