K-number	K222205
Device name	Cold Sore Device (Model: QPZ-01)
Applicant	Light Tree Ventures Europe B.V.
Product code	OKJ
Device class	Class II
Decision date	Oct 7, 2022
Decision	Substantially Equivalent
Regulation	878.4860

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View the full FDA submission: accessdata.fda.gov

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Cold Sore Device (Model: QPZ-01)

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