Medical Device Recalls
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1 result found
510(K) Number: K152777 |
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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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| ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, a... | 2 | 02/26/2021 |
FEI # 3007593903 Bovie Medical Corporation |
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