Cohero Health, LLC
Country not established
- Devices
- 1
What Cohero Health, LLC makes
Cohero Health, LLC makes SpiroThor, a device used for respiratory monitoring and spirometry testing.
SpiroThor is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
SpiroThor Ref K150137
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cohero Health, LLC have in the registry?
The registry currently lists 1 device for Cohero Health, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cohero Health, LLC's devices?
Among its 1 most recently registered device, Cohero Health, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Cohero Health, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cohero Health, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cohero Health, LLC in the registry?
The most recently registered devices listed for Cohero Health, LLC include SpiroThor.