K-number	K171666
Device name	MPR2 logO DATALOGGER
Applicant	Raumedic AG
Product code	GWM
Device class	Class II
Decision date	Jul 6, 2017
Decision	Substantially Equivalent
Regulation	882.1620

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Source

View the full FDA submission: accessdata.fda.gov

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MPR2 logO DATALOGGER

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