FDA 510(k) Application Details - K181106

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K181106
Device Name	Polymer Patient Examination Glove
Applicant	JiangSu DongXin Medical Technology Co., Ltd LongJin Road, The Economic Development Zone of SuCheng Suqian 223800 CN Other 510(k) Applications for this Company
Contact	Deng Yujie Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LZA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/26/2018
Decision Date	01/16/2019
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