K-number	K131898
Device name	A SERIES AND Q SERIES PATIENT MONITORS
Applicant	Guangdong Biolight Meditech Co., Ltd.
Product code	MWI
Device class	Class II
Decision date	Feb 18, 2014
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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A SERIES AND Q SERIES PATIENT MONITORS

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