Cardiovention, Inc.
Cardiovention, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 22, 2003.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K032068 | CARDIOVENTION CORX IOS-200 SYSTEM, MODEL IOS-200 | August 22, 2003 |
| K030141 | MODIFICATION TO CARDIOVENTION POWERBASE CONSOLE, MODEL PCB-100 | February 26, 2003 |
| K021694 | CARDIOVENTION POWERBASE CONSOLE, MODEL PBC-100 | January 8, 2003 |
| K012325 | CARDIOVENTION CORX SYSTEM, MODEL FG 0001 | April 9, 2002 |