K-number	K172965
Device name	Handheld VitalSigns Monitoring System
Applicant	Visiomed Technology Co.,Ltd
Product code	MWI
Device class	Class II
Decision date	Dec 17, 2018
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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Handheld VitalSigns Monitoring System

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