FDA 510(k) Application Details - K113837

Device Classification Name	Vinyl Patient Examination Glove   More FDA Info for this Device
510(K) Number	K113837
Device Name	Vinyl Patient Examination Glove
Applicant	HEBEI CHANGSHENG PLASTIC PRODUCTS CO., LTD. NO 99, HUANGJIN AVENUE, JULU COUNTY XINGTAI, HEBEI PROVINCE 055250 CN Other 510(k) Applications for this Company
Contact	RICHARD LU 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	12/28/2011
Decision Date	04/27/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review