GE Medical Systems Ultrasound and Primary Care Diagnostic,
Country not established
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
LOGIQ e Ref K232186
Regimes: 510(k) Registry: 510(k)LOGIQ E10s, LOGIQ Fortis Ref K231989
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ge Medical Systems Ultrasound and Primary Care Diagnostic, have in the registry?
The registry currently lists 2 devices for Ge Medical Systems Ultrasound and Primary Care Diagnostic,. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ge Medical Systems Ultrasound and Primary Care Diagnostic,'s devices?
Among its 2 most recently registered devices, Ge Medical Systems Ultrasound and Primary Care Diagnostic, has devices listed in FDA 510(k) (2 devices).
What risk classes do Ge Medical Systems Ultrasound and Primary Care Diagnostic,'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ge Medical Systems Ultrasound and Primary Care Diagnostic,'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ge Medical Systems Ultrasound and Primary Care Diagnostic, in the registry?
The most recently registered devices listed for Ge Medical Systems Ultrasound and Primary Care Diagnostic, include LOGIQ e and LOGIQ E10s, LOGIQ Fortis.