Air Liquide Healthcare America Corporation
United StatesFDA applicant, unverified
- Devices
- 4
What Air Liquide Healthcare America Corporation makes
Air Liquide Healthcare America Corporation manufactures medical oxygen delivery systems, including cryogenic oxygen concentrators like PURE CRYOGEN and portable oxygen devices such as Intelli-Ox. These products provide concentrated oxygen for therapeutic use in clinical and homecare settings, designed to improve patient oxygenation.
The company’s portfolio includes devices classified under Class I and Class II per FDA regulations, with products listed via 510(k) clearance. The manufacturer operates from the United States, adhering to domestic regulatory requirements for medical gas delivery systems.
Catalogue
Ez-Ox Plus Ref K053117
Regimes: 510(k) Registry: 510(k)Ez-Ox Plus Generation Ii Ref K131386
Regimes: 510(k) Registry: 510(k)Pure Cryogen Ref K153564
Regimes: 510(k) Registry: 510(k)Intelli-Ox Ref K161179
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Air Liquide Healthcare America Corporation have in the registry?
The registry currently lists 4 devices for Air Liquide Healthcare America Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Air Liquide Healthcare America Corporation's devices?
Among its 4 most recently registered devices, Air Liquide Healthcare America Corporation has devices listed in FDA 510(k) (4 devices).
What risk classes do Air Liquide Healthcare America Corporation's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Air Liquide Healthcare America Corporation's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Air Liquide Healthcare America Corporation in the registry?
The most recently registered devices listed for Air Liquide Healthcare America Corporation include EZ-OX PLUS, EZ-OX PLUS GENERATION II, PURE CRYOGEN and Intelli-Ox.