FDA 510(k) Application Details - K131944

Device Classification Name	Reduced- Montage Standard Electroencephalograph   More FDA Info for this Device
510(K) Number	K131944
Device Name	Reduced- Montage Standard Electroencephalograph
Applicant	JORDAN NEUROSCIENCE, INC. 1660 PLUM LANE REDLANDS, CA 92374 US Other 510(k) Applications for this Company
Contact	ANNE PERRY Other 510(k) Applications for this Contact
Regulation Number	882.1400   More FDA Info for this Regulation Number
Classification Product Code	OMC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/27/2013
Decision Date	04/10/2014
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