FDA 510(k) Application Details - K020565

Device Classification Name	Device, Galvanic Skin Response Measurement   More FDA Info for this Device
510(K) Number	K020565
Device Name	Device, Galvanic Skin Response Measurement
Applicant	VIBRANT HEALTH 150 DES GRANDS COTEAUX BEOEIL, QUEBEC J3G 2C9 CA Other 510(k) Applications for this Company
Contact	STEPHEN EMOND 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	02/20/2002
Decision Date	04/30/2002
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