Novarix Limited
United KingdomFDA applicant, unverified
- Devices
- 1
What Novarix Limited makes
Novarix Limited manufactures the IV-eye, a device designed for intravenous infusion applications in medical settings.
The IV-eye is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
IV-eye Ref K152088
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Novarix Limited have in the registry?
The registry currently lists 1 device for Novarix Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Novarix Limited's devices?
Among its 1 most recently registered device, Novarix Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Novarix Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Novarix Limited's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Novarix Limited in the registry?
The most recently registered devices listed for Novarix Limited include IV-eye.