Medical Device Recalls
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1 result found
510(K) Number: K023217 |
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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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The device is Labeled as SMART Control TRANSHEPATIC BILIARY STENT REF (PRODUCT NUMBER LISTED), VARIO... | 2 | 04/02/2003 | Cordis Corporation |
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