Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K110133 |
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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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Cordis EMPIRA NC RX PTCA Dilatation Catheter | 2 | 08/28/2014 | Cordis Corporation |
Cordis EMPIRA RX PTCA Dilatation Catheter | 2 | 08/28/2014 | Cordis Corporation |
Cordis EMPIRA RX PTCA Dilatation Catheter Catalog # 85R30300S For cardiovascular use. | 2 | 06/11/2014 | Cordis Corporation |
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