Medical Device Recalls
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1 result found
510(K) Number: K082074 |
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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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Cryogenic probe for cardiac ablation surgery, packaged individually in Tyvek pouches Product Usag... | 2 | 12/30/2014 | Atricure Inc |
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