FDA 510(k) Application Details - K012104

Device Classification Name	Surgeon'S Gloves   More FDA Info for this Device
510(K) Number	K012104
Device Name	Surgeon'S Gloves
Applicant	BEIJING REAGENT LATEX PRODUCTS CO., LTD. NO. 30 SOUTH SANLITUN ROAD, DONGDAQIAO CHAOWAI, BEIJING, P.R. 100020 CN Other 510(k) Applications for this Company
Contact	WANG YANNAN Other 510(k) Applications for this Contact
Regulation Number	878.4460   More FDA Info for this Regulation Number
Classification Product Code	KGO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/05/2001
Decision Date	08/21/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review