Ultimate Contour, Ultimate Contour Mini— 510(k) K171052

Name: FDA 510(k) clearance K171052
Creator: U.S. Food and Drug Administration
Published: 2017-10-20

Substantially Equivalent

CAO Group, Inc.

FDA 510(k) clearance K171052 for Ultimate Contour, Ultimate Contour Mini, Substantially Equivalent on 2017-10-20. Applicant: CAO Group, Inc.. Device class: 2.

Clearance details

Applicant: CAO Group, Inc.
Product code: Code PBX
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2017-04-10
Decision date: 2017-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Jordan, UT, 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.