Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Airlife with 76 510(k) clearances. The most recent is a 510(k) clearance dated Mar 5, 1984: VOLUME VENTILATOR CIRCUIT W/WATER TRAP.
| Mar 5, 1984 | VOLUME VENTILATOR CIRCUIT W/WATER TRAPK834570 · BZO | 510(k) clearances |
| Mar 5, 1984 | AQUA TRAPK834573 · BYH | 510(k) clearances |
| Dec 12, 1983 | SINGLE USE NEBULIZER-ADJUST-AIR ENTRAINK834077 · CAF | 510(k) clearances |
| Nov 3, 1983 | VOLUME VENTILATOR CIRCUIT-NEBULIZERK833196 · CAI | 510(k) clearances |
| Oct 28, 1983 | TRACH SWIVE/CONNECTORK833197 · BTR | 510(k) clearances |
| Sep 20, 1983 | DUAL DIAL VENTURI STYLE MASKK832725 · BYF | 510(k) clearances |
| Jul 26, 1983 | WHISTLER IN-LINE PRESSURE RELEASE VALVEK831246 · CBP | 510(k) clearances |
| Apr 28, 1983 | SINGLE USE NEBULIZER, ADJUST. AIR-K830895 · CAF | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
