FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Contour ProtégéAI+

K Number: K253270 · Decision Mar 27, 2026
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
45
Applicant Total
22
Review Days
179

Basic Information

Device Name
Contour ProtégéAI+
K Number
K253270
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mim Software, Inc.
Date Received
September 29, 2025
Decision Date
March 27, 2026
Product Code
QKB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QKB Radiological Image Processing Software For Radiation Therapy

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Other Clearances by Mim Software, Inc.

K Number Device Name
K251883 MIM – LesionID Pro
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K243012 MIM – Symphony HDR Fusion
K233620 MIM - Centiloid Scaling
K232862 MIM – Monte Carlo Dosimetry
K232514 MIM – Dose Analysis
K231765 Contour ProtégéAI
K223774 Contour ProtégéAI
K223800 MIM – Additional Tracers
K220256 MIM-Ablation
Search all 22 clearances from Mim Software, Inc. →