FDA 510(k) Application Details - K240266

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K240266
Device Name	Latex Patient Examination Glove
Applicant	Sri Trang Gloves (Thailand) Public Company Limited 110 Kanjanavanit Road Hatyai 90230 TH Other 510(k) Applications for this Company
Contact	M. Jordan Smith 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	01/31/2024
Decision Date	09/09/2024
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