Eliav, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Eliav, Ltd. makes
Eliav, Ltd. manufactures the PortPro electronic portal imaging system, a device used for real-time imaging and alignment verification in radiation therapy to ensure precise delivery of treatment to patients.
The company’s product portfolio is regulated under Class II devices in the U.S. and is listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Portpro Electronic Portal Imaging System Ref K964485
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eliav, Ltd. have in the registry?
The registry currently lists 1 device for Eliav, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eliav, Ltd.'s devices?
Among its 1 most recently registered device, Eliav, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Eliav, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eliav, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eliav, Ltd. in the registry?
The most recently registered devices listed for Eliav, Ltd. include PORTPRO ELECTRONIC PORTAL IMAGING SYSTEM.