Last synced on 25 January 2026 at 3:41 am

MammoScreen

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192854
510(k) Type
Traditional
Applicant
Therapixel
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/25/2020
Days to Decision
173 days
Submission Type
Summary

MammoScreen

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192854
510(k) Type
Traditional
Applicant
Therapixel
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/25/2020
Days to Decision
173 days
Submission Type
Summary