K-number	K210965
Device name	reVive Light Therapy Essentials
Applicant	Led Technologies, Inc.
Product code	OHS
Device class	Class II
Decision date	Dec 15, 2021
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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reVive Light Therapy Essentials

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