Elaitra, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Elaitra, Ltd. makes
Elaitra, Ltd. manufactures ViewFinder Software Version 1.1, a diagnostic software tool designed for medical imaging analysis and visualization.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) registry. Elaitra, Ltd. is based in the United States.
Catalogue
ViewFinder Software Version 1.1 Ref K223501
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Elaitra, Ltd. have in the registry?
The registry currently lists 1 device for Elaitra, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Elaitra, Ltd.'s devices?
Among its 1 most recently registered device, Elaitra, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Elaitra, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Elaitra, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elaitra, Ltd. in the registry?
The most recently registered devices listed for Elaitra, Ltd. include ViewFinder Software Version 1.1.