Last synced on 16 August 2024 at 11:05 pm

Centrix FluoroSilver Silver Diamine Fluoride 38%

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222459
510(k) Type
Traditional
Applicant
Centrix Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2023
Days to Decision
438 days
Submission Type
Summary

Centrix FluoroSilver Silver Diamine Fluoride 38%

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222459
510(k) Type
Traditional
Applicant
Centrix Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2023
Days to Decision
438 days
Submission Type
Summary