FDA 510(k) Applications Submitted by KENNY H.N. LIEW

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.


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