FDA 510(k) Application Details - K020360

Device Classification Name	Device, Galvanic Skin Response Measurement   More FDA Info for this Device
510(K) Number	K020360
Device Name	Device, Galvanic Skin Response Measurement
Applicant	MERIDIAN CO., LTD. 9FI SEOIL BLDG 222 JAMSILBON-DONG SONGPA-GU, SEOUL KR Other 510(k) Applications for this Company
Contact	SOO-RANG LEE 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	02/04/2002
Decision Date	08/29/2002
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