K-number	K152121
Device name	NuVent EM Sinus Dilation System
Applicant	Medtronic Xomed, Inc.
Product code	LRC
Device class	Class I
Decision date	Dec 1, 2015
Decision	Substantially Equivalent
Regulation	874.4420

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View the full FDA submission: accessdata.fda.gov

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NuVent EM Sinus Dilation System

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