K-number	K101694
Device name	HANDHELD PULSE OXIMETER MODEL M800
Applicant	Guangdong Biolight Meditech Co., Ltd.
Product code	DQA
Device class	Class II
Decision date	Sep 8, 2010
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 M800

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