Medical Device Recalls
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1 result found
510(K) Number: K061593 |
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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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Atricure Inc., Max1 Isolator Transpolar Pen. Model A000163. Used to ablate cardiac tissues during... | 2 | 03/06/2013 | Atricure Inc |
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