K-number	K161938
Device name	Fingertip Pulse Oximeter
Applicant	Xuzhou Yongkang Electronic Science Technology Co., Ltd.
Product code	DQA
Device class	Class II
Decision date	May 8, 2017
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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Fingertip Pulse Oximeter

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