Medical Device Recalls
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1 result found
510(K) Number: K963397 |
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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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Boston Scientific, Ultra-thin" Diamond" Balloon Dilatation Catheters, M001164040 (DT/3-4/5/40, 16-... | 2 | 03/25/2010 | Boston Scientific Corporation |
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