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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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