K-number	K220381
Device name	Diode Laser Therapy Systems
Applicant	Beijing Lasertell Medical Co., Ltd.
Product code	GEX
Device class	Class II
Decision date	May 20, 2022
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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