K-number	K231876
Device name	MultiPulse HoPLUS
Applicant	Asclepion Laser Technologies GmbH
Product code	GEX
Device class	Class II
Decision date	Feb 22, 2024
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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MultiPulse HoPLUS

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