K-number	K023059
Device name	UNIDUS MALE LATEX CONDOM
Applicant	Unidus Corp.
Product code	HIS
Device class	Class II
Decision date	Dec 12, 2002
Decision	Substantially Equivalent
Regulation	884.5300

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View the full FDA submission: accessdata.fda.gov

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UNIDUS MALE LATEX CONDOM

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