FDA 510(k) Applications Submitted by TEKMEDIC (M) SDN BHD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K000555	02/18/2000	TEKMEDIC POWDERED SINGLE-USE LATEX PATIENT EXAMINATION GLOVES WITH PROTEIN & POWDER LABEL CLAIM CONTAINS 70MGM OR LESS O	TEKMEDIC (M) SDN BHD
K013317	10/04/2001	TEKMEDIC POWDER-FREE WITH PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS)	TEKMEDIC (M) SDN BHD
K994250	12/16/1999	TEKMEDIC POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)	TEKMEDIC (M) SDN BHD
K971949	05/28/1997	POWDER-FREE PATIENT EXAMINATION GLOVES	TEKMEDIC (M) SDN BHD
K100694	03/11/2010	COLORED POWDER FREE AND POLYMER COATED EXAMINATION GLOVE (BLUE, BLACK AND PINK) WITH A PROTEIN CLAIM OF LESS THAN	TEKMEDIC (M) SDN BHD
K121192	04/19/2012	NITRILE EXAMINATION GLOVES (WHITE, BLUE AND BLACK)	TEKMEDIC (M) SDN BHD
K121591	05/31/2012	FLAVORED POWDER FREE AND POLYMER COATED EXAMINATION GLOVE (VANLLA, GRAPE AND STRAWBERRY)	TEKMEDIC (M) SDN BHD
K121592	05/31/2012	POWDER FREE BLUE NITRILE EXAMINATION GLOVE TESTED WITH CHEMOTHERAPY DRUGS	TEKMEDIC (M) SDN BHD
K121594	05/31/2012	COLORED POWDER FREE LATEX EXAMINATION GLOVE (WHITE AND BLUE)	TEKMEDIC (M) SDN BHD