Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K170188 |
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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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| Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS, BVX-044-BPP, BVX-150-BPP, B... | 2 | 05/20/2020 |
FEI # 3007593903 Bovie Medical Corporation |
| J-Plasma Precise(R), Catalog Numbers: BVX-150B, BVX-150N, BVX-330B, BVX- 330N, BVX-450B, BVX-450N | 2 | 03/21/2018 |
FEI # 3007593903 Bovie Medical Corporation |
| J-Plasma Precise 360(R), Catalog Numbers: BVX-330BR, BVX-330NR, BVX-450BR, BVX-450NR | 2 | 03/21/2018 |
FEI # 3007593903 Bovie Medical Corporation |
| J-Plasma Precise(R) FLEX, Catalog Number: BVX-500BF | 2 | 03/21/2018 |
FEI # 3007593903 Bovie Medical Corporation |
| J-Plasma Precise(R) OPEN, Catalog Numbers: BVX-044-BPP, BVX-044-BPS, BVX-150-BPP, BVX-150-BPS | 2 | 03/21/2018 |
FEI # 3007593903 Bovie Medical Corporation |
| J-Plasma(R) Handpiece, Catalog Numbers: GS-018C, GS-270C, BVX-270B | 2 | 03/21/2018 |
FEI # 3007593903 Bovie Medical Corporation |
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