K-number	K210168
Device name	Diode Laser Therapy Systems
Applicant	Beijing Kes Biology Technology Co., Ltd.
Product code	GEX
Device class	Class II
Decision date	May 10, 2021
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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Diode Laser Therapy Systems

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