FDA 510(k) Application Details - K220155

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K220155
Device Name	Polymer Patient Examination Glove
Applicant	Motex Healthcare (Anhui) Co., Ltd. Xinhang Economic Development Zone, Guangde County Xuancheng City 242234 CN Other 510(k) Applications for this Company
Contact	Jen Ke-Min 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	01/19/2022
Decision Date	05/23/2022
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