K-number	K200284
Device name	R-Sensor, R-Sensor
Applicant	Remedi Co., Ltd.
Product code	MUH
Device class	Class II
Decision date	Feb 28, 2020
Decision	Substantially Equivalent
Regulation	872.1800

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View the full FDA submission: accessdata.fda.gov

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R-Sensor, R-Sensor

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