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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K162820
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Arrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IABP NA/AJLA, Product Code IAP-0701 1 06/26/2020 FEI # 3015859709
Arrow International Inc
Arrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IABP NA/EMEA, Product Code IAP-0700 1 06/26/2020 FEI # 3015859709
Arrow International Inc
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