FDA 510(k) Application Details - K211601

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K211601
Device Name	Latex Patient Examination Glove
Applicant	WRP Asia Pacific SDN. BHD. Lot 1, Jalan 3, Kawasan Perusahaan Bandar Baru Salak Tinggi Sepang 43900 MY Other 510(k) Applications for this Company
Contact	Siti Syamimie Atirah Binti Mat 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	05/24/2021
Decision Date	08/22/2022
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