K-number	K121174
Device name	XPRESS MULTI-SINUS DILATION TOOL
Applicant	Entellus Medical, Inc.
Product code	LRC
Device class	Class I
Decision date	May 17, 2012
Decision	Substantially Equivalent
Regulation	874.4420

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View the full FDA submission: accessdata.fda.gov

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XPRESS MULTI-SINUS DILATION TOOL

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