Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K162820 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Arrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IABP NA/AJLA, Product Code IAP-0701 | 1 | 06/26/2020 | Arrow International Inc |
Arrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IABP NA/EMEA, Product Code IAP-0700 | 1 | 06/26/2020 | Arrow International Inc |
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