Odvi
FranceFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Stethoflux Ref K060064
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Odvi have in the registry?
The registry currently lists 1 device for Odvi. Devices recorded under merged duplicate company entries are counted once.
Which registries list Odvi's devices?
Among its 1 most recently registered device, Odvi has devices listed in FDA 510(k) (1 device).
What risk classes do Odvi's devices fall under?
Among its 1 most recently registered device, the classes recorded for Odvi's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Odvi in the registry?
The most recently registered devices listed for Odvi include STETHOFLUX.