Cleared Traditional

K253270 - Contour ProtégéAI+ (FDA 510(k) Clearance)

Mar 2026
Decision
179d
Days
Class 2
Risk

K253270 is an FDA 510(k) clearance for the Contour ProtégéAI+. This device is classified as a Radiological Image Processing Software For Radiation Therapy (Class II - Special Controls, product code QKB).

Submitted by Mim Software, Inc. (Cleveland, US). The FDA issued a Cleared decision on March 27, 2026, 179 days after receiving the submission on September 29, 2025.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050. To Provide Semi-automatic Or Fully-automated Radiological Image Processing And Analysis Tools For Radiation Therapy. Software Implementing Artificial Intelligence (ai) Including Nonadaptive Machine Learning Algorithms Trained With Clinical And/or Artificial Radiological Images. In These Devices, The Algorithm Training Images Typically Impact Device Performance. Ai Based Radiological Image Processing Software Is Intended To Be Used In The Workflow Of Radiation Therapy. Adaptive Ai Algorithms Are Not Within The Scope Of This Product Code. Primary Radiation Dose Calculation Or Plan Optimization For Treatment Planning Are Not Within Scope Of This Product Code..

Submission Details

510(k) Number K253270 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2025
Decision Date March 27, 2026
Days to Decision 179 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code QKB - Radiological Image Processing Software For Radiation Therapy
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.2050
Definition To Provide Semi-automatic Or Fully-automated Radiological Image Processing And Analysis Tools For Radiation Therapy. Software Implementing Artificial Intelligence (ai) Including Nonadaptive Machine Learning Algorithms Trained With Clinical And/or Artificial Radiological Images. In These Devices, The Algorithm Training Images Typically Impact Device Performance. Ai Based Radiological Image Processing Software Is Intended To Be Used In The Workflow Of Radiation Therapy. Adaptive Ai Algorithms Are Not Within The Scope Of This Product Code. Primary Radiation Dose Calculation Or Plan Optimization For Treatment Planning Are Not Within Scope Of This Product Code.