MERIDIAN-PORTABLE


Device Classification Name

device, galvanic skin response measurement

510(k) Number K010897
Device Name MERIDIAN-PORTABLE
Original Applicant
MERIDIAN CO., LTD.
9fi seoil bldg
222 jamsilbon-dong
songpa-gu, seoul, 

KR

Original Contact soo-rang lee
Regulation Number 882.1540
Classification Product Code
GZO  
Date Received 03/26/2001
Decision Date 06/19/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

Type Traditional
Reviewed by Third Party No

Combination Product

No