Medical Device Recalls
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1 result found
510(K) Number: K031777 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| S.M.A.R.T. CONTROL Transhepatic Biliary Stent. The Self-Expanding Nitinol Biliary Stent is delivere... | 2 | 02/15/2012 |
FEI # 1016427 Cordis Corporation |
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