Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K965236 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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 |
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 |
-