AutoContour (RADAC V5)

FDA 510(k) K260509 · Radformation, Inc.

Substantially Equivalent

510(k) numberK260509

Submission

Device name
AutoContour (RADAC V5)
Applicant
Radformation, Inc.
New York, NY, US
Received
February 17, 2026
Decision date
March 19, 2026
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
QKB – Radiological Image Processing Software For Radiation Therapy
Device class
Class II (moderate risk)
Regulation
21 CFR 892.2050
Specialty
Radiology

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…

Other 510(k)s with product code QKB

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K262452AutoContour (RADAC V6)QKB · Special Radformation, Inc.08/14/2026SE
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K260528OncoStudioQKB · Traditional Oncosoft. Inc.,07/02/2026SE
K252548AI-Rad Companion Organs RTQKB · Traditional Siemens Healthcare GmbH04/10/2026SE
K252190DeepBT Detector-PlusQKB · Traditional Aitewan Biomedical Technology, Inc.04/10/2026SE
K253270Contour ProtégéAI+QKB · Traditional Mim Software, Inc.03/27/2026SE
K251306Seg Pro V3 (RT-300)QKB · Traditional Ever Fortune.Ai, Co., Ltd.01/28/2026SE
K251351AccuContour 4.0QKB · Traditional Manteia Technologies Co., Ltd.01/23/2026SE
K250780ARTAssistantQKB · Traditional Manteia Technologies Co., Ltd.12/05/2025SE
K250427TAIMedImg DeepMetsQKB · Traditional Taiwan Medical Imaging Co., Ltd.05/28/2025SE

More from Taiwan Medical Imaging Co., Ltd.

510(k)DeviceDecision
K261718EZFluence (RADEZ V2)IYE · Traditional 08/31/2026SE
K262452AutoContour (RADAC V6)QKB · Special 08/14/2026SE
K253962ClearCheck (RADCC V2.7)IYE · Traditional 04/03/2026SE
K252988ChartCheck (RADCH V1.6)IYE · Traditional 01/05/2026SE
K252863ClearCalc Model RADCA V2.6MUJ · Traditional 12/19/2025SE
K242729AutoContour (Model RADAC V4)QKB · Traditional 12/09/2024SE
K230685AutoContour Model RADAC V3QKB · Special 04/14/2023SE
K220598AutoContour Model RADAC V2QKB · Traditional 08/24/2022SE
K220583ClearCheck Model RADCC V2IYE · Traditional 08/23/2022SE
K220582ClearCalc Model RADCA V2MUJ · Traditional 08/22/2022SE

Questions and answers

When was AutoContour (RADAC V5) cleared by the FDA?

AutoContour (RADAC V5) (K260509) received a 510(k) decision of Substantially Equivalent on March 19, 2026, 30 days after the submission was received.

What is the product code of K260509?

The FDA product code is QKB – Radiological Image Processing Software For Radiation Therapy, a Class II (moderate risk) device regulated under 21 CFR 892.2050.