K-number	K131876
Device name	M SERIES PATIENT MONITOR
Applicant	Mid-Link Consulting Co, Ltd.
Product code	MHX
Device class	Class II
Decision date	Feb 27, 2014
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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M SERIES PATIENT MONITOR

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