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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 33 of 33 Results
510(K) Number: K181122
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FDA Recall
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Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, ... 1 08/30/2023 Datascope Corp.
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, ... 1 08/30/2023 Datascope Corp.
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, ... 1 08/30/2023 Datascope Corp.
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