FDA 510(k) Applications Submitted by NULATEX SDN. BHD.

FDA 510(k) Number Submission Date Device Name Applicant
K132107 07/08/2013 MALE LATEX CONDOM NULATEX SDN. BHD.
K070937 04/04/2007 MULTIPLE BRAND MALE LATEX CONDOM NULATEX SDN. BHD.
K121241 04/25/2012 MALE LATEX CONDOM NULATEX SDN. BHD.


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