FDA 510(k) Application Details - K162405

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K162405
Device Name	Polymer Patient Examination Glove
Applicant	COMFORT RUBBER GLOVES INDUSTRIES SDN BHD LOT 821, JALAN MATANG MATANG 84750 MY Other 510(k) Applications for this Company
Contact	CHAN YEW MEN 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	08/29/2016
Decision Date	03/28/2017
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