Medical Device Recalls
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1 result found
510(K) Number: K974684 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Boston Scientific Wiseguide Guide Catheter 7F, .076 '', Femoral Approach, Manufactured for Boston S... | 2 | 06/10/2006 |
FEI # 3002095335 Boston Scientific |
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