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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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