K-number	K112877
Device name	COMEN MULTI-PARAMETER PATIENT MONITOR
Applicant	Goldway (Us), Inc.
Product code	MWI
Device class	Class II
Decision date	Nov 7, 2012
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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COMEN MULTI-PARAMETER PATIENT MONITOR

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