FDA 510(k) Application Details - K151679

Device Classification Name	Vinyl Patient Examination Glove   More FDA Info for this Device
510(K) Number	K151679
Device Name	Vinyl Patient Examination Glove
Applicant	HEZE YUZE GLOVE CO., LTD NO. 1 HANJIANG ROAD CAOXIAN 274415 CN Other 510(k) Applications for this Company
Contact	LILY ZHU 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	06/22/2015
Decision Date	11/27/2015
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