K-number	K152898
Device name	DIODE LASER THERAPY SYSTEMS
Applicant	Beijing Sincoheren Science and Tech. Development Co., Ltd.
Product code	GEX
Device class	Class II
Decision date	Feb 9, 2016
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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DIODE LASER THERAPY SYSTEMS

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