FDA 510(k) Application Details - K223375

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K223375
Device Name	Polymer Patient Examination Glove
Applicant	Kossan International Sdn Bhd3 Wisma Kossan, Lot 782, Jalan Sungai Putus Off Batu 3 3/4, Jalan Kapar Klang 42100 MY Other 510(k) Applications for this Company
Contact	Cho Sow Fong 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	11/04/2022
Decision Date	03/15/2023
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