FDA 510(k) Application Details - K023771

Device Classification Name	Electroencephalograph   More FDA Info for this Device
510(K) Number	K023771
Device Name	Electroencephalograph
Applicant	NEUROSCAN 7850 PASEO DEL NORTE SUITE 101 EL PASO, TX 79912 US Other 510(k) Applications for this Company
Contact	ELVIRA GARCIA Other 510(k) Applications for this Contact
Regulation Number	882.1400   More FDA Info for this Regulation Number
Classification Product Code	GWQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/12/2002
Decision Date	02/06/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review