Cardiac Assist, Maquet Cardiovascular, LLC
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K112372 | CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP | September 15, 2011 |
| K112327 | SENSATION(TM) PLUS 8FR. 50CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES | September 9, 2011 |