K-number	K021975
Device name	LASERSYSTEM BEAUTYSTAR 532
Applicant	Asclepion-Meditec AG
Product code	GEX
Device class	Class II
Decision date	Sep 13, 2002
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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LASERSYSTEM BEAUTYSTAR 532

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