DIZZYFIX— 510(k) K081602

Name: FDA 510(k) clearance K081602
Creator: U.S. Food and Drug Administration
Published: 2008-09-19

Substantially Equivalent

Clearwater Clinical Limited

FDA 510(k) clearance K081602 for DIZZYFIX, Substantially Equivalent on 2008-09-19. Applicant: Clearwater Clinical Limited. Device class: Unclassified.

Clearance details

Applicant: Clearwater Clinical Limited
Product code: Code LXV
Device class: Unclassified
Advisory panel: Unknown
Date received: 2008-06-06
Decision date: 2008-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Calgary, Alberta, CA

Download summary PDF View on FDA.gov ↗

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