K-number	K071560
Device name	PROVENT NASAL DILATOR, MODEL BR2
Applicant	Ventus Medical, Inc.
Product code	OHP
Device class	Class II
Decision date	Feb 8, 2008
Decision	Substantially Equivalent
Regulation	872.5570

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View the full FDA submission: accessdata.fda.gov

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PROVENT NASAL DILATOR, MODEL BR2

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