K200323 is an FDA 510(k) clearance for the AutoContour. This device is classified as a Radiological Image Processing Software For Radiation Therapy (Class II - Special Controls, product code QKB).
Submitted by Radformation, Inc. (New York, US). The FDA issued a Cleared decision on October 30, 2020, 263 days after receiving the submission on February 10, 2020.
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..