K-number	K170538
Device name	RVS-100 Vital Signs Monitor
Applicant	Rudolf Riester GmbH
Product code	MWI
Device class	Class II
Decision date	Oct 17, 2017
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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RVS-100 Vital Signs Monitor

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