Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K121442 |
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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 POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is intended to dilate stenoses in ilia... | 2 | 11/06/2018 | Cordis Corporation |
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-... | 2 | 01/16/2015 | Cordis Corporation |
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