FDA 510(k) Application Details - K101133

Device Classification Name	Device, Monitoring, Intracranial Pressure   More FDA Info for this Device
510(K) Number	K101133
Device Name	Device, Monitoring, Intracranial Pressure
Applicant	DPCOM AS 435 RICE CREEK TERRACE FRIDLEY, MN 55432 US Other 510(k) Applications for this Company
Contact	CONSTANCE BUNDY Other 510(k) Applications for this Contact
Regulation Number	882.1620   More FDA Info for this Regulation Number
Classification Product Code	GWM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/22/2010
Decision Date	11/18/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review