Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K163542 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-31, 0998-00-0800-32, 099... | 2 | 09/30/2021 | Datascope Corp. |
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