GE Healthcare Information Technologies
Country not established
- Devices
- 3
What GE Healthcare Information Technologies makes
Ge Healthcare Information Technologies develops laboratory information management systems, including the Centricity AW Suite Option, which integrates with clinical workflows to support diagnostic reporting and data management in pathology settings.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) premarket notifications. The manufacturer operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Centricity Aw Suite Option Ref K061372
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ge Healthcare Information Technologies have in the registry?
The registry currently lists 3 devices for Ge Healthcare Information Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ge Healthcare Information Technologies's devices?
Among its 3 most recently registered devices, Ge Healthcare Information Technologies has devices listed in FDA 510(k) (3 devices).
What risk classes do Ge Healthcare Information Technologies's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ge Healthcare Information Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ge Healthcare Information Technologies in the registry?
The most recently registered devices listed for Ge Healthcare Information Technologies include MODIFICATION TO: MAC 5500 RESTING ECG ANALYSIS SYSTEM, Mac-Lab Recording Systems AltiX, CardioLab Recording Systems AltiX, ComboLab Recording Systems AltiX, MLCL Client Software AltiX and CENTRICITY AW SUITE OPTION.