FDA 510(k) Application Details - K993202

Device Classification Name	Device, Galvanic Skin Response Measurement   More FDA Info for this Device
510(K) Number	K993202
Device Name	Device, Galvanic Skin Response Measurement
Applicant	GENERAL DEVICES 1000 RIVER ST. RIDGEFIELD, NJ 07657 US Other 510(k) Applications for this Company
Contact	MICHAEL SMITH 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	09/24/1999
Decision Date	12/17/1999
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