Last synced on 25 January 2026 at 3:41 am

MIM – LesionID Pro

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251883
510(k) Type
Traditional
Applicant
Mim Software, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2025
Days to Decision
174 days
Submission Type
Summary

MIM – LesionID Pro

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251883
510(k) Type
Traditional
Applicant
Mim Software, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2025
Days to Decision
174 days
Submission Type
Summary