K-number	K132038
Device name	ACCUTORR 7 VITAL SIGNS MONITOR
Applicant	Mindray North America
Product code	MWI
Device class	Class II
Decision date	May 2, 2014
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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ACCUTORR 7 VITAL SIGNS MONITOR

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