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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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