FDA 510(k) Application Details - K212401

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K212401
Device Name	Polymer Patient Examination Glove
Applicant	Inner Mongolia Cureguard Medical Technology Co.,Ltd. Room 326, Management Committee of New Industrial Park, Tumote Youqi Baotou 014100 CN Other 510(k) Applications for this Company
Contact	Guo Hua 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	08/02/2021
Decision Date	10/25/2021
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