FDA 510(k) Application Details - K203622

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K203622
Device Name	Polymer Patient Examination Glove
Applicant	Beijing Biosis Healing Biological Technology Co., Ltd. Valley No.1 Bio-medicine Industry Park, Daxing District Beijing 102600 CN Other 510(k) Applications for this Company
Contact	Ting Jiang 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	12/11/2020
Decision Date	08/20/2021
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