Sonic Incytes
CanadaFDA applicant, unverified
- Devices
- 4
What Sonic Incytes makes
Sonic Incytes makes Velacur and Liver Incytes, Model 1005, which are medical devices used for diagnostic or monitoring purposes.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Velacur Ref K233977
Regimes: 510(k) Registry: 510(k)Liver Incytes, Model 1005 Ref K201597
Regimes: 510(k) Registry: 510(k)Velacur Ref K223287
Regimes: 510(k) Registry: 510(k)Velacur Ref K232459
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sonic Incytes have in the registry?
The registry currently lists 4 devices for Sonic Incytes. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonic Incytes's devices?
Among its 4 most recently registered devices, Sonic Incytes has devices listed in FDA 510(k) (4 devices).
What risk classes do Sonic Incytes's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Sonic Incytes's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sonic Incytes in the registry?
The most recently registered devices listed for Sonic Incytes include Velacur and Liver Incytes, Model 1005.