Liquid Technology Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Liquid Technology Corp. makes
Liquid Technology Corp. manufactures medical gas mixtures, including lung diffusion, laser, and blood gas blends designed for clinical and procedural use. These products are formulated to support respiratory therapy, surgical applications, and diagnostic testing by delivering precise gas compositions.
The company’s portfolio is regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. Products are listed in the FDA’s 510(k) registry, and the company operates from the United States.
Catalogue
Lung Diffusion Mixture Ref K954542
Regimes: 510(k) Registry: 510(k)Laser Gas Mixture Ref K954544
Regimes: 510(k) Registry: 510(k)Blood Gas Mixture Ref K954546
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Liquid Technology Corp. have in the registry?
The registry currently lists 3 devices for Liquid Technology Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Liquid Technology Corp.'s devices?
Among its 3 most recently registered devices, Liquid Technology Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Liquid Technology Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Liquid Technology Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Liquid Technology Corp. in the registry?
The most recently registered devices listed for Liquid Technology Corp. include LUNG DIFFUSION MIXTURE, LASER GAS MIXTURE and BLOOD GAS MIXTURE.