K-number	K242202
Device name	LightWalker Laser System Family
Applicant	Fotona D.O.O.
Product code	GEX
Device class	Class II
Decision date	Aug 23, 2024
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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LightWalker Laser System Family

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