FDA 510(k) Application Details - K111308

Device Classification Name	Device, Galvanic Skin Response Measurement   More FDA Info for this Device
510(K) Number	K111308
Device Name	Device, Galvanic Skin Response Measurement
Applicant	ZYTO TECHNOLOGIES, INC 387 SOUTH 520 WEST SUITE 200 LINDON, UT 84042 US Other 510(k) Applications for this Company
Contact	VAUGHN R COOK Other 510(k) Applications for this Contact
Regulation Number	882.1540   More FDA Info for this Regulation Number
Classification Product Code	GZO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/10/2011
Decision Date	08/30/2011
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