Medical Device Recalls
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1 result found
510(K) Number: K071309 |
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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 BLUE MAX" 20 Balloon Dilatation Catheter, UPN M001125420 (BMQ/7-4/5.8/40, 12-542),... | 2 | 03/25/2010 | Boston Scientific Corporation |
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