FDA 510(k) Application Details - K212309

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K212309
Device Name	Latex Patient Examination Glove
Applicant	Sri Trang Gloves (Thailand) Public Company Limited 10 SOi 10 Phetkasem Road Hatyai 90110 TH Other 510(k) Applications for this Company
Contact	Jarinya Jirojkul Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LYY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/23/2021
Decision Date	04/08/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review