P-Cure, Ltd.
IsraelFDA 510(k) applicant, unverified
- Devices
- 4
What P-Cure, Ltd. makes
P-Cure, Ltd. makes proton beam therapy systems, including the P-Cure Proton Beam Therapy System, P-Cure Proton Therapy System (PPTS), and related models such as P-ARTIS and P-ART, MODEL 001. These devices are designed for delivering proton radiation therapy in clinical settings.
The devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
P-Cure Proton Beam Therapy System Ref K221996
510(k) 510(k)P-Artis Ref K160611
510(k) 510(k)P-Cure Proton Therapy System (PPTS) Ref K242418
510(k) 510(k)P-Art, Model 001 Ref K092424
510(k) 510(k)
Frequently asked questions
How many devices does P-Cure, Ltd. have in the registry?
The registry currently lists 4 devices for P-Cure, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list P-Cure, Ltd.'s devices?
Among its 4 most recently registered devices, P-Cure, Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do P-Cure, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for P-Cure, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from P-Cure, Ltd. in the registry?
The most recently registered devices listed for P-Cure, Ltd. include P-Cure Proton Beam Therapy System, P-ARTIS, P-Cure Proton Therapy System (PPTS) and P-ART, MODEL 001.