GE Medical Systems Europe
FranceFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Autobone Ref K031871
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ge Medical Systems Europe have in the registry?
The registry currently lists 1 device for Ge Medical Systems Europe. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ge Medical Systems Europe's devices?
Among its 1 most recently registered device, Ge Medical Systems Europe has devices listed in FDA 510(k) (1 device).
What risk classes do Ge Medical Systems Europe's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ge Medical Systems Europe's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ge Medical Systems Europe in the registry?
The most recently registered devices listed for Ge Medical Systems Europe include AUTOBONE.