K-number	K002032
Device name	C02 LASER MULTIPULSE
Applicant	Asclepion-Meditec AG
Product code	GEX
Device class	Class II
Decision date	Sep 11, 2000
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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C02 LASER MULTIPULSE

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