FDA 510(k) Application Details - K182640

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K182640
Device Name	Polymer Patient Examination Glove
Applicant	Shandong Hengya Packaging Printing Co.,Ltd Hetou village, Yingqiu town, Changle county, Weifang City 262416 CN Other 510(k) Applications for this Company
Contact	Sunny Hu 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	09/24/2018
Decision Date	04/12/2019
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