K-number	K150175
Device name	HeatLux Pro I
Applicant	Home Skinovations , Ltd.
Product code	ILY
Device class	Class II
Decision date	Mar 31, 2015
Decision	Substantially Equivalent
Regulation	890.5500

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View the full FDA submission: accessdata.fda.gov

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HeatLux Pro I

Everything you need for a 510(k) submission. Nothing you don't.