K-number	K121697
Device name	FINGERTIP PULSE OXIMETER
Applicant	Andon Health Co, Ltd.
Product code	DQA
Device class	Class II
Decision date	Oct 15, 2012
Decision	Substantially Equivalent
Regulation	870.2700

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Source

View the full FDA submission: accessdata.fda.gov

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FINGERTIP PULSE OXIMETER

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