Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of AbbottLabelled by claude-sonnet-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 13, 2026, FDA's public records list Oximetrix with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jan 13, 1986: MODEL 3000 OPTICATH COMPUTER.
| Date | Record | Source |
|---|---|---|
| Jan 13, 1986 | MODEL 3000 OPTICATH COMPUTERK853018 · DXG | 510(k) clearances |
| Oct 23, 1984 | HEMO STATIC/ESU SCALPEL SYSTEMK842622 · GEI | 510(k) clearances |
| Jan 25, 1984 | PUMP INFUSION WEARABLE INFUSION PUMPK833966 · JSJ | 510(k) clearances |
| Nov 1, 1982 | OPTICATH HEPARIN COATED, FLOW-DIRECTK823007 · DYG | 510(k) clearances |
| May 18, 1982 | FLOW DIRECTED THERMAL-DILUTION CATHETERK821056 · | 510(k) clearances |
| May 18, 1982 | FLOW DIRECTED THERMAL-DILUTION INFUSIONK821057 · DYG | 510(k) clearances |
| Mar 25, 1982 | OPTICATHK820674 · DQE | 510(k) clearances |
| Jul 20, 1981 | OXIMETRIX ACCU SAT CPBK811391 · DRY | 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
