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., part of Chart IndustriesLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list AirSep Corporation with 19 510(k) clearances. The most recent is a 510(k) clearance dated Dec 18, 2015: Deployable Oxygen Generation System-Smaill (DOGS-S).
| Dec 18, 2015 | Deployable Oxygen Generation System-Smaill (DOGS-S)K150930 · CAW | 510(k) clearances |
| Mar 28, 2011 | CENTROX, RELIANT, ULTROX, AS-D+, AS-E, AS-G, AS-J, AS-K AND AS-LK101154 · CAW | 510(k) clearances |
| Oct 9, 2008 | OXISCAN II DATA MANAGEMENT SYSTEMK080348 · DQA | 510(k) clearances |
| Mar 13, 2002 | LIFESTYLE OXYGEN CONCENTRATORK020324 · CAW | 510(k) clearances |
| Jan 17, 2002 | HEALTHLIFE OXYGEN CONCENTRATOR MODEL AS009K012037 · CAW | 510(k) clearances |
| Oct 20, 2000 | DA VINCHI EEG AND EMG/EP SYSTEMSK000963 · GWF | 510(k) clearances |
| Aug 31, 2000 | IMPULSE SELECTK001579 · NFB | 510(k) clearances |
| Aug 1, 2000 | DA VINCHI EMG/EP ISA1004EPK001467 · GWE | 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
