K-number	K133891
Device name	MULTIPULSE TM+1470
Applicant	Asclepion Laser Technologies GmbH
Product code	GEX
Device class	Class II
Decision date	Jan 30, 2015
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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MULTIPULSE TM+1470

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