Cardiac Assist Devices, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K012520 | GYRO-TIP LARIAT DEFLECTABLE LOOP MAPPING CATHETER, MODEL GTL-20E | March 27, 2002 |
| K960849 | MAGNO ALARM | March 26, 1997 |
| K955847 | GYRO TIP EP CATHETER | January 29, 1997 |