NuFACE FIX Skin Toning Device— 510(k) K182424

Name: FDA 510(k) clearance K182424
Creator: U.S. Food and Drug Administration
Published: 2018-12-18

Substantially Equivalent

Carol Cole Company Dba Nuface

FDA 510(k) clearance K182424 for NuFACE FIX Skin Toning Device, Substantially Equivalent on 2018-12-18. Applicant: Carol Cole Company Dba Nuface. Device class: 2.

Clearance details

Applicant: Carol Cole Company Dba Nuface
Product code: Code NFO
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2018-09-06
Decision date: 2018-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vista, CA, 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.