Thoratec Switzerland GMBH
3 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| 2nd Generation CentriMag Primary Console, REF: 201-90401, 201-90701, 201-90411, 201-90421, recall (Z-2215-2024) | Thoratec Switzerland GMBH | 2024-06-27 |
| CentriMag Acute Circulatory Support System Motor, U.S. Model 102956 and OUS Model 201-1000 recall (Z-0221-2020) | Thoratec Switzerland GMBH | 2019-10-30 |
| Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumpi recall (Z-0103-2019) | Thoratec Switzerland GMBH | 2018-10-12 |
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Every clearance here is in the API, with alerts when new ones post.