K-number	K133810
Device name	VC150 VITAL SIGNS MONITOR
Applicant	Innokas Yhtyma
Product code	MWI
Device class	Class II
Decision date	Oct 30, 2014
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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VC150 VITAL SIGNS MONITOR

Everything you need for a 510(k) submission. Nothing you don't.