VERTIGONE BPPV GOGGLE— 510(k) K082634

Name: FDA 510(k) clearance K082634
Creator: U.S. Food and Drug Administration
Published: 2009-04-07

Substantially Equivalent

Vertigone, Inc.

FDA 510(k) clearance K082634 for VERTIGONE BPPV GOGGLE, Substantially Equivalent on 2009-04-07. Applicant: Vertigone, Inc.. Device class: Unclassified.

Clearance details

Applicant: Vertigone, Inc.
Product code: Code LXV
Device class: Unclassified
Advisory panel: Unknown
Date received: 2008-09-10
Decision date: 2009-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodlands, TX, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.