Medical Device Recalls
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1 result found
510(K) Number: K113213 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 20-Pole LASSO Nav Catheter Eco, Catalog # D-1349-02S. Designed to facilitate electrophysiological... | 2 | 06/28/2013 |
FEI # 3003113629 Biosense Webster, Inc. |
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