K-number	K163509
Device name	XprESS ENT Dilation System
Applicant	Entellus Medical, Inc.
Product code	PNZ
Device class	Class II
Decision date	Apr 5, 2017
Decision	Substantially Equivalent
Regulation	874.4180

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Source

View the full FDA submission: accessdata.fda.gov

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XprESS ENT Dilation System

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