FDA 510(k) Application Details - K030737

Device Classification Name	Neuroimaging Correlation Software For Electroencephalograph Or Magnetoencephalograph   More FDA Info for this Device
510(K) Number	K030737
Device Name	Neuroimaging Correlation Software For Electroencephalograph Or Magnetoencephalograph
Applicant	CTF SYSTEMS (2001), INC. 15-1750 MCLEAN AVE. PORT COQUITLAM, B.C. V3C 1M9 CA Other 510(k) Applications for this Company
Contact	DARYL WISDAHL Other 510(k) Applications for this Contact
Regulation Number	882.1400   More FDA Info for this Regulation Number
Classification Product Code	OLX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/10/2003
Decision Date	10/10/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review