FDA 510(k) Application Details - K060910

Device Classification Name	Vinyl Patient Examination Glove   More FDA Info for this Device
510(K) Number	K060910
Device Name	Vinyl Patient Examination Glove
Applicant	JIANGSU EVERYGUARD PLASTIC PRODUCTS CO., LTD RM 1606 BLDG 1JIANZIANG YUAN NO 209 BEI SI HUAN SHONG RD HA BEIJING CN Other 510(k) Applications for this Company
Contact	CHU XIA OAN Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LYZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/03/2006
Decision Date	06/07/2006
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