NuFace Trinity Plus Device— 510(k) K201782
Substantially EquivalentCarol Cole Company Dba Nuface
FDA 510(k) clearance K201782 for NuFace Trinity Plus Device, Substantially Equivalent on 2021-01-22. Applicant: Carol Cole Company Dba Nuface.
Clearance details
- Applicant
- Carol Cole Company Dba Nuface
- Product code
- Code NFO
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Vista, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.