NUFACE MINI DEVICE— 510(k) K133823

Substantially Equivalent

Carol Cole Company

FDA 510(k) clearance K133823 for NUFACE MINI DEVICE, Substantially Equivalent on 2014-04-17. Applicant: Carol Cole Company. Device class: 2.

Clearance details

Applicant: Carol Cole Company
Product code: Code NFO
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2013-12-17
Decision date: 2014-04-17
Decision: Substantially Equivalent
Clearance type: Abbreviated
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.