Cardiac Assist, Maquet Cardiovascular, LLC
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K112372 | CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP | DSP | 2011-09-15 | View |
| 510(k) | K112327 | SENSATION(TM) PLUS 8FR. 50CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES | DSP | 2011-09-09 | View |
No matching devices.
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