K-number	K151947
Device name	LightSheer Desire Light Laser System
Applicant	Lumenis, Ltd.
Product code	GEX
Device class	Class II
Decision date	Aug 12, 2015
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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LightSheer Desire Light Laser System

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