K-number	K172792
Device name	Handheld Pulse Oximeter, Model SP-20
Applicant	Shenzhen Creative Industry Co., Ltd.
Product code	DQA
Device class	Class II
Decision date	Nov 13, 2018
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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Handheld Pulse Oximeter, Model SP-20

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