K-number	K093007
Device name	ENTELLUS MEDICAL BALLOON DEVICE
Applicant	Entellus Medical, Inc.
Product code	LRC
Device class	Class I
Decision date	Feb 5, 2010
Decision	Substantially Equivalent
Regulation	874.4420

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View the full FDA submission: accessdata.fda.gov

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ENTELLUS MEDICAL BALLOON DEVICE

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