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Raumedic AG

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250285NEUROVENT-P (092946-003); NEUROVENT (092956-003); NEUROVENT-IFD-R (095317-003); NEUROVENT-IFD-S (091August 29, 2025
K171666MPR2 logO DATALOGGERJuly 6, 2017
K130529RAUMEDIC-PTO-MONITORING-SYSTEMOctober 25, 2013
K120252RAUMEDIC-ICP-TEMP-MONITORING-SYSTEMApril 11, 2012
K112017RAUMEDIC ICP MONITORING SYSTEMOctober 11, 2011
K103206RAUMEDIC- ICP-MONITORING SYSTEMMarch 4, 2011