K-number	K151644
Device name	Masimo Root Vital Signs Monitoring System and Accessories
Applicant	Masimo Corporation
Product code	MWI
Device class	Class II
Decision date	Feb 12, 2016
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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Masimo Root Vital Signs Monitoring System and Accessories

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