FDA 510(k) Application Details - K161422

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K161422
Device Name	Polymer Patient Examination Glove
Applicant	WRP ASIA PACIFIC SDN. BHD. LOT 1, JALAN 3, KAW PERUSAHAAN BANDAR BARU SALAK TINGGI, SEPANG 43900 MY Other 510(k) Applications for this Company
Contact	SARALA DEVI JAYARAMAN 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	05/23/2016
Decision Date	10/20/2016
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