Clearance Summary
Contour ProtégéAI+ received FDA 510(k) clearance under submission number K250035, sponsored by Mim Software, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-02-03.
- Submission: K250035
- Applicant / Sponsor: Mim Software, Inc.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2025-02-03
Classification & Regulation
This clearance is catalogued under FDA product code QKB and 21 CFR 892.2050, within the Radiology review panel as a Class II device.