K-number	K031007
Device name	KWIKEZE MALE CONDOM APPLICATOR
Applicant	Condax, LLC
Product code	HIS
Device class	Class II
Decision date	Nov 14, 2003
Decision	Substantially Equivalent
Regulation	884.5300

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View the full FDA submission: accessdata.fda.gov

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KWIKEZE MALE CONDOM APPLICATOR

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