Medical Device Recalls
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1 result found
510(K) Number: K130559 |
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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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Biosense Webster MobiCath Bi-Directional Guiding Sheath, Model D140010 (small curve) and D140011 (la... | 2 | 07/29/2017 | Greatbatch Medical |
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