K-number	K191088
Device name	Checkme O2 Pulse Oximeter
Applicant	Shenzhen Viatom Technology Co., Ltd.
Product code	DQA
Device class	Class II
Decision date	Dec 2, 2019
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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Checkme O2 Pulse Oximeter

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