K-number	K181121
Device name	Beurer IPL 5500 device/ IPL 5000/ IPL PureSkin Pro
Applicant	Home Well Trading, Ltd.
Product code	OHT
Device class	Class II
Decision date	Jun 28, 2018
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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Beurer IPL 5500 device/ IPL 5000/ IPL PureSkin Pro

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