Elekta Oncology Systems, Ltd.
Country not established
- Devices
- 5
What Elekta Oncology Systems, Ltd. makes
Elekta Oncology Systems, Ltd. manufactures radiation therapy systems, including the Synergy System for linear accelerator-based treatments, and electronic portal imaging devices (EPID) such as the iView and modified ViewGT models for real-time imaging during radiotherapy planning and delivery. The company also produces the RT Desktop, a software platform for radiation therapy workflow management and treatment planning.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The company is based in the United States and its products are listed in the FDA’s 510(k) registry.
Catalogue
Elekta Synergy System Ref K032996
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Rt Desktop Ref K982713
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Elekta Oncology Systems, Ltd. have in the registry?
The registry currently lists 5 devices for Elekta Oncology Systems, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Elekta Oncology Systems, Ltd.'s devices?
Among its 5 most recently registered devices, Elekta Oncology Systems, Ltd. has devices listed in FDA 510(k) (5 devices).
What risk classes do Elekta Oncology Systems, Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Elekta Oncology Systems, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elekta Oncology Systems, Ltd. in the registry?
The most recently registered devices listed for Elekta Oncology Systems, Ltd. include ELEKTA SYNERGY SYSTEM, ELEKTA ONCOLOGY SYSTEMS ICOM/QUICKMODE SOFTWARE OPTIONS, MODIFICATION TO: VIEWGT ELECTRONIC PORTAL IMAGING DEVICE (EPID) and RT DESKTOP.