FDA 510(k) Applications Submitted by SUPERMAX GLOVE MANUFACTURING SDN BHD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K010198	01/22/2001	STERILE POWDERED LATEX SURGEON GLOVES	SUPERMAX GLOVE MANUFACTURING SDN BHD
K000644	02/25/2000	SUPERGLOVES STERILE POWDERED LATEX EXAMINATION GLOVES	SUPERMAX GLOVE MANUFACTURING SDN BHD
K013589	10/30/2001	CHLORINATED POWDER FREE LATEX MEDICAL EXAMINATION GLOVES WITH ALOE VERA	SUPERMAX GLOVE MANUFACTURING SDN BHD
K013953	11/30/2001	AURELIA CHLORINATED POWDER FREE LATEX MEDICAL EXAMINATION GLOVES WITH ALOE VERA AND GINSENG WITH PROTEIN LABELING CLAIM	SUPERMAX GLOVE MANUFACTURING SDN BHD
K024083	12/11/2002	GREEN POWDER FREE NITRILE MEDICAL EXAMINATION GLOVES WITH PEPPERMINT FLAVOR	SUPERMAX GLOVE MANUFACTURING SDN BHD
K014230	12/26/2001	STERILE POWDER FREE LATEX SURGEON GLOVES WITH PROTEIN LABELING CLAIM (50 MICROGRAM OR LESS)	SUPERMAX GLOVE MANUFACTURING SDN BHD