FDA 510(k) Applications Submitted by MEDIPURE CORPORATION (M) SDN. BHD.

FDA 510(k) Number Submission Date Device Name Applicant
K001165 04/10/2000 POLYMER COATED POWDER FREE, LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS) MEDIPURE CORPORATION (M) 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.


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