K-number	K192491
Device name	Coolief Radiofrequency Generator (CRG) System
Applicant	Avanos Medical, Inc.
Product code	GXD
Device class	Class II
Decision date	Feb 21, 2020
Decision	Substantially Equivalent
Regulation	882.4400

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Source

View the full FDA submission: accessdata.fda.gov

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Coolief Radiofrequency Generator (CRG) System

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