K-number	K222555
Device name	reepot Nd; YAG laser system
Applicant	Ilooda Co,., Ltd.
Product code	GEX
Device class	Class II
Decision date	Sep 23, 2022
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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reepot Nd; YAG laser system

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