Verisci Corporation
Country not established
- Devices
- 1
What Verisci Corporation makes
Verisci Corporation manufactures the NEUCODIA device, a Class II medical product designed for neurological monitoring or intervention, though specific clinical applications are not detailed.
The NEUCODIA device is regulated under the FDA’s 510(k) pathway as a Class II product and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Neucodia Ref K081591
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Verisci Corporation have in the registry?
The registry currently lists 1 device for Verisci Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Verisci Corporation's devices?
Among its 1 most recently registered device, Verisci Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Verisci Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Verisci Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Verisci Corporation in the registry?
The most recently registered devices listed for Verisci Corporation include NEUCODIA.