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FDA 510(k) Applications Submitted by GOH S KHEK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K981159
03/31/1998
PROFLEX POWDER FREE NITRILE EXAMINATION GLOVES
LATEXX PARTNERS BHD.
K981767
05/19/1998
QTEXX POWDERFREE LATEX EXAMINATION GLOVES
LATEXX PARTNERS BHD.
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