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 Rescue IntraAortic Balloon Pump. Model UDI 0998-00-0800-75 1060756711... | 1 | 12/30/2021 | Datascope Corp. |
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