FDA 510(k) Application Details - K212029

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K212029
Device Name	Polymer Patient Examination Glove
Applicant	Taizhou Kangjian Medical Equipments Co., Ltd. The Machine Electricity Zone (Hang Ni Kan) of Yuhuan County Taizhou 317600 CN Other 510(k) Applications for this Company
Contact	Hua Cong 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	06/29/2021
Decision Date	11/16/2021
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