FDA 510(k) Applications Submitted by FLEXITECH SDN. BHD.

FDA 510(k) Number Submission Date Device Name Applicant
K990499 02/17/1999 PREPOWDERED NITRILE EXAMINATION GLOVES FLEXITECH SDN. BHD.
K990502 02/17/1999 PREPOWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (100 MICROGRAMS OR LESS) FLEXITECH SDN. BHD.
K990495 02/17/1999 POWDER FREE NITRILE EXAMINATION GLOVES FLEXITECH SDN. BHD.
K990501 02/17/1999 POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM FLEXITECH SDN. BHD.
K994354 12/23/1999 POLYMER COATED, POWDER FREE, LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS) FLEXITECH SDN. BHD.
K994416 12/29/1999 POLYMER COATED POWDER FREE NITRILE EXAMINATION GLOVES, BLUE FLEXITECH SDN. BHD.


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