K-number	K223262
Device name	Renuvion® APR Handpiece
Applicant	Apyx Medical Corporation
Product code	GEI
Device class	Class II
Decision date	Feb 23, 2023
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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Renuvion® APR Handpiece

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