K-number	K191542
Device name	Apyx Plasma/RF Handpiece
Applicant	Bovie Medical Corporation Dba Apyx Medical Corporation
Product code	GEI
Device class	Class II
Decision date	Oct 11, 2019
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Apyx Plasma/RF Handpiece

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