FDA 510(k) Application Details - K013926

Device Classification Name	Needle, Acupuncture, Single Use   More FDA Info for this Device
510(K) Number	K013926
Device Name	Needle, Acupuncture, Single Use
Applicant	WUJIANG CITY SHENLI MEDICAL AND HEALTH MATERIAL CO 503 ROOM, 8 BUILDING, 600 LIU ZHON ROAD SHANGHI 200233 CN Other 510(k) Applications for this Company
Contact	GONG BO Other 510(k) Applications for this Contact
Regulation Number	880.5580   More FDA Info for this Regulation Number
Classification Product Code	MQX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/28/2001
Decision Date	07/18/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review