Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K965236 |
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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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Datascope System 98/98xt, CS 100/CS100i and CS 300 Intra-Aortic Balloon Pump. The Intra-Aortic B... | 1 | 05/21/2014 | Maquet Datascope Corp - Cardiac Assist Division |
Datascope/ Maquet IABPs. System 98/98XT Intra-Aortic Balloon Pump; CS100/CS100i Intra-Aortic Ball... | 1 | 06/13/2011 | Maquet Datascope Corp - Cardiac Assist Division |
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