FDA 510(k) Applications Submitted by APL PRODUCTS SDN. BHD.

FDA 510(k) Number Submission Date Device Name Applicant
K020865 03/18/2002 ONLINE POWDER FREE, LATEX EXAMINATION GLOVES APL PRODUCTS SDN. BHD.
K990879 03/16/1999 PRE POWDERED LATEX EXAMINATION GLOVES APL PRODUCTS SDN. BHD.
K990901 03/18/1999 POWDER FREE LATEX EXAMINATION GLOVES APL PRODUCTS SDN. BHD.


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