GE Healthcare, Breas Medical AB
SwedenFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Vivo 50 Ref K123144
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ge Healthcare, Breas Medical AB have in the registry?
The registry currently lists 1 device for Ge Healthcare, Breas Medical AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ge Healthcare, Breas Medical AB's devices?
Among its 1 most recently registered device, Ge Healthcare, Breas Medical AB has devices listed in FDA 510(k) (1 device).
What risk classes do Ge Healthcare, Breas Medical AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ge Healthcare, Breas Medical AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ge Healthcare, Breas Medical AB in the registry?
The most recently registered devices listed for Ge Healthcare, Breas Medical AB include VIVO 50.