FDA 510(k) Applications Submitted by PRISCILLA WEE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040176	01/26/2004	MAXTER POWDER FREE NITRILE MEDICAL EXAMINATION GLOVES	MAXTER GLOVE MANUFACTURING SDN BHD
K032467	08/11/2003	MAXTER STERILE POWDERED LATEX SURGICAL GLOVES	MAXTER GLOVE MANUFACTURING SDN BHD
K013774	11/13/2001	CHLORINATED POWDER FREE NITRILE MEDICAL EXAMINATION GLOVES WITH ALOE VERA	SUPERMAX SDN BHD