Medical Device Recalls
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1 result found
510(K) Number: K083919 |
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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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Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152 AMP020150152 AMP02512015... | 2 | 11/06/2015 | Medtronic Vascular, Inc. |
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