FDA 510(k) Applications Submitted by MULTISAFE SDN BHD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K062526	08/28/2006	BLUE POWDERED LATEX EXAMINATION GLOVES, NON-STERILE	MULTISAFE SDN BHD
K062527	08/28/2006	BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE	MULTISAFE SDN BHD
K011293	04/30/2001	POWDER FREE POLYMER COATED LATEX MEDICAL EXAMINATION GLOVES, NON-STERILE W/ PROTEIN CONTENT LABELING CLAIM 50 MCG OR LES	MULTISAFE SDN BHD
K001497	05/15/2000	MULTISAFE-POWDERED NITRILE GLOVES, NON-STERILE (BLUE)	MULTISAFE SDN BHD
K000999	03/28/2000	MULTISAFE POWDER-FREE PATIENT LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)	MULTISAFE SDN BHD
K001619	05/25/2000	MULTISAFE POWDER FREE NITRILE GLOVES, NON STERILE (BLUE)	MULTISAFE SDN BHD
K993811	11/10/1999	MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE	MULTISAFE SDN BHD