Last synced on 12 July 2024 at 11:04 pm

NuFACE Mini Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191672
510(k) Type
Traditional
Applicant
Carol Cole Company dba NuFACE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2019
Days to Decision
113 days
Submission Type
Summary

NuFACE Mini Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191672
510(k) Type
Traditional
Applicant
Carol Cole Company dba NuFACE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2019
Days to Decision
113 days
Submission Type
Summary