Skip to the page

Data / Medical devices / United States / Airgas Usa LLC

Airgas Usa LLC: FDA-registered device maker in Salem, NH, United States, 1 510(k) clearance

Airgas Usa LLC is registered with the FDA (registration 1250022) in Salem, NH, 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 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
1250022
FEI number
1216783
Address
17 Northwestern Dr, Salem, NH, United States, 03079
Owner or operator
Airgas USA LLC (9009904)
Roles
Manufacturer
First device listed
August 21, 1996
Registered through
2026
Brand names listed
1. Biological Atmosphere (Aerobic), 2. Biological Atmosphere ( Anaerobic), 3. Blood Gas, 4. Lung Diffusion Gas, 5. Pulmonary Function Mixture, 7. Calibration Gas Mixture, 8. Laser Gas, Laser Gas

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, 1992K924796LUNG DIFFUSION 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.