Medical Device Recalls
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1 result found
510(K) Number: K823487 |
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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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Bard Fluoro-4 Silicone Ureteral Stent, Bard® Fluoro-4", Silicone Ureteral Coil Stent; Bard® Silicone... | 2 | 11/14/2016 | C.R. Bard, Inc. |
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