K-number	K173067
Device name	LightForce LTS Model 1000, 1500, 2500, and 4000
Applicant	Litecure, LLC
Product code	GEX
Device class	Class II
Decision date	Feb 22, 2018
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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LightForce LTS Model 1000, 1500, 2500, and 4000

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