FDA 510(k) Application Details - K212002

Device Classification Name	Vinyl Patient Examination Glove   More FDA Info for this Device
510(K) Number	K212002
Device Name	Vinyl Patient Examination Glove
Applicant	Yunnan Huazhiyuan Medical Technology Co., Ltd. Yangjie Industrial Park,Jianshui County Honghe Hani and Yi Autonomous Prefecture 654300 CN Other 510(k) Applications for this Company
Contact	Yun Gao 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	06/28/2021
Decision Date	09/23/2021
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