K-number	K123792
Device name	HORIZON XVU (FFR)
Applicant	Mennen Medical , Ltd.
Product code	DQX
Device class	Class II
Decision date	Aug 30, 2013
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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HORIZON XVU (FFR)

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