K-number	K203812
Device name	Oxyfit Pulse Oximeter
Applicant	Shenzhen Viatom Technology Co., Ltd.
Product code	DQA
Device class	Class II
Decision date	Nov 8, 2022
Decision	Substantially Equivalent
Regulation	870.2700

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Source

View the full FDA submission: accessdata.fda.gov

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Oxyfit Pulse Oximeter

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