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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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