The following data is part of a premarket notification filed by Bovie Medical Corporation with the FDA for Bovie J-plasma Precise 360 Handpiece.
| Device ID | K152570 |
| 510k Number | K152570 |
| Device Name: | Bovie J-Plasma Precise 360 Handpiece |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | BOVIE MEDICAL CORPORATION 5115 ULMERTON ROAD Clearwater, FL 33760 |
| Contact | Brian Kunst |
| Correspondent | Brian Kunst BOVIE MEDICAL CORPORATION 5115 ULMERTON ROAD Clearwater, FL 33760 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-09-09 |
| Decision Date | 2015-11-02 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10607151010758 | K152570 | 000 |
| 10607151010741 | K152570 | 000 |
| 10607151010734 | K152570 | 000 |
| 10607151010727 | K152570 | 000 |