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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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