GE Hungary Kft
Country not established
- Devices
- 2
What GE Hungary Kft makes
Ge Hungary Kft manufactures medical simulation software tools for radiotherapy planning, including CT atlas-based contouring and re-planning capabilities. Their products also include MR-based segmentation for pelvic organs at risk, designed to assist in precise treatment planning for radiation therapy.
These devices fall under Class II regulatory classification and are listed via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ge Hungary Kft have in the registry?
The registry currently lists 2 devices for Ge Hungary Kft. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ge Hungary Kft's devices?
Among its 2 most recently registered devices, Ge Hungary Kft has devices listed in FDA 510(k) (2 devices).
What risk classes do Ge Hungary Kft's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ge Hungary Kft's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ge Hungary Kft in the registry?
The most recently registered devices listed for Ge Hungary Kft include ADVANTAGESIM MD WITH CT ATLAS-BASED CONTOURING AND RE-PLANNING OPTIONS and ADVANTAGESIM MD MR PELVIC ORGAN AT RISK SEGMENTATION.