K-number	K143541
Device name	Relieva SpinPlus Balloon Sinuplasty System
Applicant	Acclarent, Inc.
Product code	LRC
Device class	Class I
Decision date	Apr 22, 2015
Decision	Substantially Equivalent
Regulation	874.4420

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Source

View the full FDA submission: accessdata.fda.gov

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Relieva SpinPlus Balloon Sinuplasty System

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