Medical Device Recalls
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1 result found
510(K) Number: K101345 |
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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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| EZ STEER Catheter D-1267-04-S / 8mm Non-Navigation Bi-Directional Catheter Cardiovascular cathete... | 2 | 05/22/2012 |
FEI # 3003113629 Biosense Webster, Inc. |
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