AIRGAS USA LLC

FDA Device Registration & Listing · Elk Grove Village, IL, US · Registration 3004931173

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004931173
FEI Number
3008852974
Entity Name
AIRGAS USA LLC
City/State/Country
Elk Grove Village, IL, US
Establishment Address
1601 NICHOLAS BLVD., Elk Grove Village, IL 60007, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AIRGAS USA, LLC (Owner Number: 9066386)
Owner / Operator Contact Address
1250 W. Washington St, --, West Chicago, IL 60185, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Laser Gas Pulmonary Function Mixture Blood Gas Biological Atmosphere (Anaerobic) Lung Diffusion Gas Mixture Blood Gas Mixture, Lung Diffusion Calibration Gas Mixtures Biological Atmosphere (Aerobic) Laser Gas

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BXK Gas, Calibration (Specified Concentration) Anesthesiology Class 1 868.6400 2004-09-03
NXF Gas, Laser Generating General, Plastic Surgery Class 1 878.4810 2009-02-19

Official Correspondent

Amy Selode

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AIRGAS USA, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3007313217 Airgas USA, LLC. La Porte, TX, US
1645341 AIRGAS USA, LLC TULSA, OK, US
1033831 AIRGAS USA, LLC. ATL, GA, US
2127612 AIRGAS USA LLC Waukesha, WI, US
1056791 AIRGAS USA, LLC. TEMPLE TERRACE, FL, US

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2529486 Linde Gas & Equipment Inc. BETHLEHEM, PA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004931173. Last updated year: 2026. Please use registration number 3004931173 when referencing this establishment in official correspondence.
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