FDA 510(k) Application Details - K072276

Device Classification Name	Electrode, Needle   More FDA Info for this Device
510(K) Number	K072276
Device Name	Electrode, Needle
Applicant	XIAN FRIENDSHIP ELECTRONICS CO.,LTD. RM 1606 BLDG. 1, JIANXIANG YUA NO. 229 BEI SI HUAN ZHONG RD. HAIDIAN DISTRICT, BEIJING 100083 CN Other 510(k) Applications for this Company
Contact	CHU XIAOAN Other 510(k) Applications for this Contact
Regulation Number	882.1350   More FDA Info for this Regulation Number
Classification Product Code	GXZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/15/2007
Decision Date	05/16/2008
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