Air Liquide Healthcare
Country not established
- Devices
- 1
What Air Liquide Healthcare makes
Air Liquide Healthcare manufactures the Intelli-Ox, a medical oxygen therapy device designed to monitor and deliver precise oxygen levels to patients.
The Intelli-Ox is classified as a Class I device and is listed under the FDA’s 510(k) pathway. The company operates from the United States.
Catalogue
Intelli-Ox Ref K143060
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Air Liquide Healthcare have in the registry?
The registry currently lists 1 device for Air Liquide Healthcare. Devices recorded under merged duplicate company entries are counted once.
Which registries list Air Liquide Healthcare's devices?
Among its 1 most recently registered device, Air Liquide Healthcare has devices listed in FDA 510(k) (1 device).
What risk classes do Air Liquide Healthcare's devices fall under?
Among its 1 most recently registered device, the classes recorded for Air Liquide Healthcare's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Air Liquide Healthcare in the registry?
The most recently registered devices listed for Air Liquide Healthcare include Intelli-Ox.