K-number	K203441
Device name	The Alma Hybrid Laser System
Applicant	Alma Lasers , Ltd.
Product code	GEX
Device class	Class II
Decision date	Jul 2, 2021
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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The Alma Hybrid Laser System

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