Medical Device Recalls
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1 result found
510(K) Number: K133607 |
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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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InterValve V8 Balloon Aortic Valvuloplasty Catheter, model 172212C110, 192412C110, 212612C110, 2328... | 2 | 05/15/2014 | InterValve Inc |
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