Medical Device Recalls
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1 result found
510(K) Number: K111766 |
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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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IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System... | 2 | 06/18/2013 | IDEV Technologies, Inc. |
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