K-number	K163135
Device name	Finger Pulse Oximeter
Applicant	Shenzhen Fitfaith Technology Co.,Ltd
Product code	DQA
Device class	Class II
Decision date	Sep 19, 2017
Decision	Substantially Equivalent
Regulation	870.2700

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Source

View the full FDA submission: accessdata.fda.gov

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Finger Pulse Oximeter

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