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FDA PRODUCT CODE · CLASS II

QKBRadiological Image Processing Software For Radiation Therapy

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.

DEVICE CLASS
Class II
REGULATION
21 CFR 892.2050
MEDICAL SPECIALTY
Radiology
REVIEW PANEL
RA
ImplantLife-sustainingGMP-exemptThird-party review eligible
17
510(K)/PMA CLEARANCES
510k: 17
0
RECALL ENTRIES

Recent clearances

K261306Varian Medical Systems · 510k2026-07-10
K260528Oncosoft. Inc., · 510k2026-07-02
K252190Aitewan Biomedical Technology, Inc. · 510k2026-04-10
K252548Siemens Healthcare GmbH · 510k2026-04-10
K253270Mim Software, Inc. · 510k2026-03-27
K260509Radformation, Inc. · 510k2026-03-19
K251306Ever Fortune.Ai, Co., Ltd. · 510k2026-01-28
K251351Manteia Technologies Co., Ltd. · 510k2026-01-23

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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