FDA 510(k) K151325, Bovie J-Plasma Handpiece, by Bovie Medical Corporation

510(K) Number: K151325
Device Name: Bovie J-Plasma Handpiece
Manufacturer: Bovie Medical Corporation
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 05/18/2015
Decision Date: 08/04/2015
Regulation Medical Specialty: General & Plastic Surgery