FDA 510(k) Application Details - K013498

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K013498
Device Name	Latex Patient Examination Glove
Applicant	MAXTER GLOVE MANUFACTURING SDN BHD 6TH MILES OFF JALAN MERU KLANG SELANGOR 41050 MY Other 510(k) Applications for this Company
Contact	STANLEY THAI 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	10/22/2001
Decision Date	01/17/2002
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