FDA 510(k) Applications Submitted by GOH SEE 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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