Maquet Cardiovascular
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Maquet HEARTSTRING Aortic Cutter 4.3 mm, AC-3043, Lot numbers 9081071 and 9082071, Manufac recall (Z-1222-2011) | Maquet Cardiovascular | 2011-02-11 |
| Maquet Coronary Perfusion Cannulae with Balloon Tip, with either self-inflating balloon ti recall (Z-1869-2009) | Maquet Cardiovascular | 2009-08-31 |
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Every clearance here is in the API, with alerts when new ones post.