FDA 510(k) Applications Submitted by UNIDUS CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K072747 09/27/2007 UNIDUS MAGNUM MALE LATEX CONDOM UNIDUS CORP.
K023059 09/13/2002 UNIDUS MALE LATEX CONDOM UNIDUS CORP.
K023129 09/19/2002 UNIDUS MALE LATEX CONDOM (YELLOW, PINK, GREEN & BLACK) UNIDUS CORP.
K023175 09/23/2002 UNIDUS MALE LATEX CONDOM (WITH COLOR AND FLAVORING) UNIDUS CORP.
K023176 09/23/2002 UNDUS MALE LATEX CONDOM (WITH FLAVORING) UNIDUS CORP.
K033541 11/10/2003 LONG LOVE CONDOM UNIDUS CORP.


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