Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K010874 |
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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| Mach 1 6F JR 3.5 Guide Catheter. Catalog No. 34356-685. Sterilized with ethylene oxide gas. Nonp... | 3 | 01/24/2006 |
FEI # 3002095335 Boston Scientific Scimed |
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