External Counterpulsation Lab
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K021340 | AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE | January 30, 2003 |
| K012141 | AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE | October 25, 2001 |