K-number	K110739
Device name	ENTELLUS MEDICAL SINUS GUIDEWIRE
Applicant	Entellus Medical, Inc.
Product code	LRC
Device class	Class I
Decision date	Jun 14, 2011
Decision	Substantially Equivalent
Regulation	874.4420

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Source

View the full FDA submission: accessdata.fda.gov

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ENTELLUS MEDICAL SINUS GUIDEWIRE

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