K-number	K073041
Device name	RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER
Applicant	Acclarent, Inc.
Product code	KAM
Device class	Class I
Decision date	Mar 11, 2008
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER

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