Medical Device Recalls
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1 result found
510(K) Number: K183610 |
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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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Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS, BVX-044-BPP, BVX-150-BPP, B... | 2 | 05/20/2020 | Bovie Medical Corporation |
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