K-number	K221766
Device name	Solon
Applicant	Lmg Lasers Comercio, Importacao E Exportacao Ltda
Product code	GEX
Device class	Class II
Decision date	Jan 5, 2024
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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Solon

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