FDA 510(k) Application Details - K092780

Device Classification Name	Interferential Current Therapy   More FDA Info for this Device
510(K) Number	K092780
Device Name	Interferential Current Therapy
Applicant	FUJI DYNAMICS LIMITED 23/F., UNIT 1-3, 788 CHEUNG SHA WAN ROAD KOWLOON, HONG KONG CN Other 510(k) Applications for this Company
Contact	CHING KONG LEE Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/10/2009
Decision Date	01/07/2010
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