K-number	K241155
Device name	Cold Sore Device (QPZ-03)
Applicant	Shenzhen Nuon Medical Equipment Co., Ltd.
Product code	OKJ
Device class	Class II
Decision date	Sep 5, 2024
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 (QPZ-03)

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