FDA 510(k) Application Details - K992129

Device Classification Name	Device, Galvanic Skin Response Measurement   More FDA Info for this Device
510(K) Number	K992129
Device Name	Device, Galvanic Skin Response Measurement
Applicant	PHAZX SYSTEMS, INC. 4655 KIRKWOOD COURT BOULDER, CO 80301 US Other 510(k) Applications for this Company
Contact	LEWIS W WARD 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	06/23/1999
Decision Date	09/17/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review