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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K120868
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MEGA 7.5Fr.IAB , Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation th... 2 07/21/2023 Datascope Corp.
Datascope Intra-Aortic Ballon Catheters (IABs)-MEGA 7.5Fr 30cc IAB, P/N: 0684-00-0294-01,0684-00-... 2 08/21/2020 Datascope Corporation
Datascope Intra-Aortic Ballon Catheters (IABs)-MEGA 8Fr 50cc IAB Kit P/N: 0684-00-0296-01, 0684-00-0... 2 08/21/2020 Datascope Corporation
Datascope Intra-Aortic Balloon Catheters (IABs)-MEGA 7.5Fr 40cc IAB Kit P/N: 0684-00-0295-01, 0684-0... 2 08/21/2020 Datascope Corporation
Intra-Aortic Balloon Catheter Mega 7.5FR 30cc Product Usage: The intra-aortic balloon catheter a... 2 04/16/2018 Datascope Corporation
Intra-Aortic Balloon Catheter Mega 7.5FR 40cc Product Usage: The intra-aortic balloon catheter a... 2 04/16/2018 Datascope Corporation
MEGA® 7.5Fr. 30cc Intra-Aortic Balloon Catheter with Insertion Kit & STATLOCK® MEGA® 7.5Fr. 40cc ... 2 06/08/2016 Datascope Corporation
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