Medical Device Recalls
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1 result found
510(K) Number: K033497 |
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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 Luminexx 3 Biliary Stent and Delivery System | 2 | 09/24/2005 | Bard Peripheral Vascular Inc |
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