Medical device makerLabelled by claude-haiku-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 Sequal Technologies with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 29, 2010: MESA II OXYGEN CONCENTRATOR MODEL: T2000 SERIES.
| Date | Record | Source |
|---|---|---|
| Nov 29, 2010 | MESA II OXYGEN CONCENTRATOR MODEL: T2000 SERIESK100920 · CAW | 510(k) clearances |
| Dec 31, 2009 | MESA OXYGEN CONCENTRATOR, MODEL 2-6000 SERIESK091541 · CAW | 510(k) clearances |
| Oct 20, 2009 | OMNI 2 OXYGEN SYSTEMK083163 · CAW | 510(k) clearances |
| Sep 10, 2004 | INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10K042262 · CAW | 510(k) clearances |
| Mar 27, 2002 | OMNI OXYGEN SYSTEM, MODEL 1000K013931 · CAW | 510(k) clearances |
| Jun 4, 2001 | INTEGRA OXYGEN CONCENTRATORS MODEL 6400-OMK003472 · CAW | 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
