Medical Device Recalls
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1 result found
510(K) Number: K132782 |
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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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CARTO 3 EP Navigation System and Accessories, Product Codes: FG540000 and FG540000C, Software Versio... | 2 | 09/09/2016 | Biosense Webster, Inc. |
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