Medical Device Recalls
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1 result found
510(K) Number: K063217 |
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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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Vena Tech LP Vena Cava Filter System, Item No/REF. 05010024, Model No: 40DLP, B Braun. Manufacturer:... | 2 | 11/24/2007 | B. Braun Interventional Systems |
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