FDA 510(k) Application Details - K210777

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K210777
Device Name	Polymer Patient Examination Glove
Applicant	Shandong Jieshi Medical Products Co.,Ltd North Road, Fumin Avenue, Qinghe Street, Caoxian County Heze 274400 CN Other 510(k) Applications for this Company
Contact	Li Biao 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	03/15/2021
Decision Date	11/02/2021
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