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Data / Medical devices / United States / Airgas USA, LLC

Airgas USA, LLC: FDA-registered device maker in Lansing, MI, United States, 1 510(k) clearance

Airgas USA, LLC is registered with the FDA (registration 1835566) in Lansing, MI, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 17, 1992. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
1835566
FEI number
3001237678
Address
5018 Empire Way, Lansing, MI, United States, 48917
Owner or operator
Airgas USA (1820490)
Roles
Manufacturer
First device listed
June 19, 2008
Registered through
2027
Brand names listed
Biological Atmosphere (Aerobic), Biological Atmosphere (Anaerobic), Blood Gas, Calibration Gas Mixture, Laser Gas, Lung Diffusion Gas, Pulmonary Function Mixture

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
December 17, 1992K924795BLOOD GAS MIXTUREBXKSubstantially EquivalentGulf States Airgasaccessdata.fda.gov

Compare with other makers

Updated December 17, 1992. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.