K-number	K151071
Device name	SmartLinx Vitals Plus Patient Monitoring System
Applicant	Capsule Technologie Sas
Product code	MWI
Device class	Class II
Decision date	Sep 17, 2015
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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SmartLinx Vitals Plus Patient Monitoring System

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