510(k) K253270

Device
Contour ProtégéAI+
Applicant
Mim Software, Inc.
510(k) number
K253270
Product code
QKB
Decision
Substantially Equivalent (SESE)
Decision date
2026-03-27
Date received
2025-09-29
Regulation
892.2050
Classification name
Radiological Image Processing Software For Radiation Therapy
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Sydney Lindner
Address
25800 Science Park Dr., Suite 180 Cleveland OH US 44122 44122

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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