FDA 510(k) Application Details - K970436

Device Classification Name	Device, Galvanic Skin Response Measurement   More FDA Info for this Device
510(K) Number	K970436
Device Name	Device, Galvanic Skin Response Measurement
Applicant	NATURAL HERBAL PRODUCTS, INC. 724 WIGGINS BAY DR. NAPLES, FL 34110 US Other 510(k) Applications for this Company
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	02/05/1997
Decision Date	08/15/1997
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