K-number	K120252
Device name	RAUMEDIC-ICP-TEMP-MONITORING-SYSTEM
Applicant	Raumedic AG
Product code	GWM
Device class	Class II
Decision date	Apr 11, 2012
Decision	Substantially Equivalent
Regulation	882.1620

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View the full FDA submission: accessdata.fda.gov

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RAUMEDIC-ICP-TEMP-MONITORING-SYSTEM

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