PROVENT NASAL DILATOR, MODEL BR2— 510(k) K071560

Name: FDA 510(k) clearance K071560
Creator: U.S. Food and Drug Administration
Published: 2008-02-08

Substantially Equivalent

Ventus Medical, Inc.

FDA 510(k) clearance K071560 for PROVENT NASAL DILATOR, MODEL BR2, Substantially Equivalent on 2008-02-08. Applicant: Ventus Medical, Inc.. Device class: 2.

Clearance details

Applicant: Ventus Medical, Inc.
Product code: Code OHP
Device class: Class 2
Regulation: 21 CFR 872.5570
Advisory panel: Dental
Date received: 2007-06-07
Decision date: 2008-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hillsborough, CA, US

Download summary PDF View on FDA.gov ↗

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