FDA Device Intelligence
Home › Airgas Therapeutics, LLC › Airgas USA LLC

Airgas USA LLC

Airgas Therapeutics, LLC · Model Pulmonary Function Gas · UDI-DI 00819601020139

BXK
10
510(k) clearances
8
Adverse events
0
Recalls
60
Facilities

Description

Description: 0.6% C2H2, 9% He, 21% O2, Bal. N2; Cylinder: 200; Valve: CGA 500; For use with Pulmonary Function Diagnostic Equipment in accordance with manufacturer's instructions.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.