K-number	K152570
Device name	Bovie J-Plasma Precise 360 Handpiece
Applicant	Bovie Medical Corporation
Product code	GEI
Device class	Class II
Decision date	Nov 2, 2015
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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Bovie J-Plasma Precise 360 Handpiece

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