Liquid Air Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Liquid Air Corp. makes
Liquid Air Corp. produces calibration gases for medical monitoring devices, including specific mixtures for carbon dioxide monitors and anesthetic gas calibration.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Calibration Gas For Carbon Dioxide Monitor Ref K874297
Regimes: 510(k) Registry: 510(k)Anesthetic Gas Calibration Mixture Ref K902754
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Liquid Air Corp. have in the registry?
The registry currently lists 2 devices for Liquid Air Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Liquid Air Corp.'s devices?
Among its 2 most recently registered devices, Liquid Air Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Liquid Air Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Liquid Air Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Liquid Air Corp. in the registry?
The most recently registered devices listed for Liquid Air Corp. include CALIBRATION GAS FOR CARBON DIOXIDE MONITOR and ANESTHETIC GAS CALIBRATION MIXTURE.