K-number	K203214
Device name	DemarkQ WOW, DemarkQ POP
Applicant	Shenzhen Kaiyan Medical CO , Ltd.
Product code	OLP
Device class	Class II
Decision date	Jul 22, 2021
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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DemarkQ WOW, DemarkQ POP

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