K-number	K212300
Device name	Pulse Oximeter
Applicant	Shenzhen Mericonn Technology Co., Ltd.
Product code	DQA
Device class	Class II
Decision date	Feb 25, 2022
Decision	Substantially Equivalent
Regulation	870.2700

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Source

View the full FDA submission: accessdata.fda.gov

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Pulse Oximeter

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