NuFACE Mini Device— 510(k) K191672
Substantially EquivalentCarol Cole Company Dba Nuface
FDA 510(k) clearance K191672 for NuFACE Mini Device, Substantially Equivalent on 2019-10-15. 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
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Vista, CA, US
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