NuFACE Mini Plus— 510(k) K201680
Substantially EquivalentCarole Cole Company
FDA 510(k) clearance K201680 for NuFACE Mini Plus, Substantially Equivalent on 2021-02-19. Applicant: Carole Cole Company. Device class: 2.
Clearance details
- Applicant
- Carole Cole Company
- Product code
- Code NFO
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Vista, CA, US
Recent devices under product code NFO
view allData sourced from openFDA. This site is unofficial and independent of the FDA.