FDA 510(k) Applications Submitted by T H OOI

FDA 510(k) Number Submission Date Device Name Applicant
K943880 08/09/1994 RIA LATEX CONDOM MBF PERSONAL CARE SDN. BHD.
K061551 06/05/2006 POWDER FREE LATEX EXAMINATION GLOVES, NATURAL OR BLUE COLOUR AND WITH PROTEIN CONTENT LABELING CLAIM (50 UG OR LESS) MEDIPURE CORPORATION (M) SDN. BHD.
K101645 06/11/2010 NON-CHLORINATED, POLYMER COATED POWDER FREE NATURAL RUBBER LATEX EXAMINATION GLOVES AND PROTEIN LABELING CLAIM OF LATEXX MANUFACTURING SDN.BHD.
K110418 02/14/2011 POWDER FREE NITRILE EXAMINATION GLOVES W.A. RUBBERMATE CO., LTD.


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