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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CS100 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3013-55 For cardiovascular use. | 1 | 07/16/2019 | Datascope Corp. |
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