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Raumedic AG

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K250285 NEUROVENT-P (092946-003); NEUROVENT (092956-003); NEUROVENT-IFD-R (095317-003); NEUROVENT-IFD-S (091678-003); NEUROVENT-P-TEMP (094268-003); NEUROVENT-TEMP (094278-003); NEUROVENT-TEMP-IFD-R (095327-003); NEUROVENT-TEMP-IFD-S (094288-003); NEUROVENT-PTO (095008-003); NEUROVENT-PTO 2L (095108-003); NEUROVENT-PX (091580-003); BOLT-DRILL KIT CH5 (091888-003); BOLT-DRILL KIT CH9 (091898-003); BOLT-DRILL KIT PTO (092380-003); BOLT-DRILL KIT VP 16 (092969-003); BOLT KIT CH5 (091868-003); BOLGWM2025-08-29 View
510(k) K171666 MPR2 logO DATALOGGERGWM2017-07-06 View
510(k) K130529 RAUMEDIC-PTO-MONITORING-SYSTEMGWM2013-10-25 View
510(k) K120252 RAUMEDIC-ICP-TEMP-MONITORING-SYSTEMGWM2012-04-11 View
510(k) K112017 RAUMEDIC ICP MONITORING SYSTEMGWM2011-10-11 View
510(k) K103206 RAUMEDIC- ICP-MONITORING SYSTEMGWM2011-03-04 View
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