K-number	K170777
Device name	Bovie J-Plasma Precise FLEX Handpiece
Applicant	Bovie Medical Corporation
Product code	GEI
Device class	Class II
Decision date	May 1, 2017
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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Bovie J-Plasma Precise FLEX Handpiece

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