Applied Radiation
Country not established
- Devices
- 2
What Applied Radiation makes
Applied Radiation manufactures the ARS-1000 Radiation Therapy Treatment Planning System, a device used for designing and optimizing radiation treatment plans in oncology. It integrates imaging data and dose calculations to support precise delivery of radiotherapy for cancer patients.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) clearance process. The portfolio is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Ars-1000 Ref K820448
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Applied Radiation have in the registry?
The registry currently lists 2 devices for Applied Radiation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Applied Radiation's devices?
Among its 2 most recently registered devices, Applied Radiation has devices listed in FDA 510(k) (2 devices).
What risk classes do Applied Radiation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Applied Radiation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Applied Radiation in the registry?
The most recently registered devices listed for Applied Radiation include ARS-1000 RADIATION THERAPY TREATMENT PLANNING SYSTEM and ARS-1000.