K-number	K230042
Device name	Q-Rejuvalight Pro Facewear (Model: P19-0023)
Applicant	Light Tree Ventures Europe B.V.
Product code	OHS
Device class	Class II
Decision date	Apr 28, 2023
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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Q-Rejuvalight Pro Facewear (Model: P19-0023)

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