Medical Device Recalls
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1 result found
510(K) Number: K023681 |
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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 Renegade" Hi-Flo Microcatheter, Peripheral Vascular Use. Sterilized with Ethylen... | 2 | 09/24/2009 | Boston Scientific Corporation |
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