Mgc Diagnostics Corporation
Country not established
- Devices
- 1
What Mgc Diagnostics Corporation makes
Mgc Diagnostics Corporation manufactures the Fenom Flo FeNO Monitoring System, which is a device used for the measurement of fractional exhaled nitric oxide in human breath.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Fenom Flo™ FeNO Monitoring System Ref K251674
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mgc Diagnostics Corporation have in the registry?
The registry currently lists 1 device for Mgc Diagnostics Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mgc Diagnostics Corporation's devices?
Among its 1 most recently registered device, Mgc Diagnostics Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Mgc Diagnostics Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mgc Diagnostics Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mgc Diagnostics Corporation in the registry?
The most recently registered devices listed for Mgc Diagnostics Corporation include Fenom Flo™ FeNO Monitoring System.