K-number	K221979
Device name	Pulse Oximeter (Model C101A2, C101B1, C101A3)
Applicant	Shenzhen Imdk Medical Technology Co., Ltd.
Product code	DQA
Device class	Class II
Decision date	Oct 16, 2022
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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Pulse Oximeter (Model C101A2, C101B1, C101A3)

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