Upper Four, Inc.
Country not established
- Devices
- 1
What Upper Four, Inc. makes
Upper Four, Inc. manufactures the Breathing Zone, a device designed to monitor or enhance respiratory conditions within a defined breathing area.
The Breathing Zone is classified as a Class II medical device and is listed under FDA 510(k) clearance. The company is based in the United States.
Catalogue
Breathing Zone Ref K831067
510(k) 510(k)
Frequently asked questions
How many devices does Upper Four, Inc. have in the registry?
The registry currently lists 1 device for Upper Four, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Upper Four, Inc.'s devices?
Among its 1 most recently registered device, Upper Four, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Upper Four, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Upper Four, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Upper Four, Inc. in the registry?
The most recently registered devices listed for Upper Four, Inc. include BREATHING ZONE.