FDA 510(k) Application Details - K070890

Device Classification Name	Interferential Current Therapy   More FDA Info for this Device
510(K) Number	K070890
Device Name	Interferential Current Therapy
Applicant	EVERLIFE MEDICAL EQUIPMENT CO., LTD. NO. 58, FU-CHIUN STREET HSIN CHU CITY 30067 TW Other 510(k) Applications for this Company
Contact	Ke-Min Jen 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	03/30/2007
Decision Date	06/29/2007
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