FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

RAUMEDIC-ICP-TEMP-MONITORING-SYSTEM

K Number: K120252 · Decision Apr 11, 2012
Classifications
1
FEI Numbers
65
Registration Numbers
66
Same Product Code
104
Applicant Total
6
Review Days
75

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Basic Information

Device Name
RAUMEDIC-ICP-TEMP-MONITORING-SYSTEM
K Number
K120252
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1620
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Raumedic AG
Date Received
January 27, 2012
Decision Date
April 11, 2012
Product Code
GWM
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWM Device, Monitoring, Intracranial Pressure

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GWM), ordered by most recent decision date.

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Other Clearances by Raumedic AG

K Number Device Name
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); BOL
K171666 MPR2 logO DATALOGGER
K130529 RAUMEDIC-PTO-MONITORING-SYSTEM
K112017 RAUMEDIC ICP MONITORING SYSTEM
K103206 RAUMEDIC- ICP-MONITORING SYSTEM