Medical device makerLabelled 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 15, 2026, FDA's public records list Omega Medical Electronics with 21 510(k) clearances. The most recent is a 510(k) clearance dated Jan 7, 1983: PHOSPHORUS REAGENT SET.
| Jan 7, 1983 | PHOSPHORUS REAGENT SETK823691 · CEO | 510(k) clearances |
| Jul 22, 1982 | GLUCOSE(ENZYMATIC) REAGENT SETK821204 · CGA | 510(k) clearances |
| Jul 22, 1982 | UREA NITROGEN REAGENT SETK821212 · CDW | 510(k) clearances |
| Jul 22, 1982 | SGPT-UV REAGENT SETK821206 · CKA | 510(k) clearances |
| Jul 20, 1982 | LDH-UV REAGENT SETK821201 · CFJ | 510(k) clearances |
| Jul 20, 1982 | SGOT-UV REAGENT SETK821208 · CIT | 510(k) clearances |
| Jul 20, 1982 | TRIGLYCERIDE REAGENT SETK821205 · CDT | 510(k) clearances |
| Jul 14, 1982 | SGOT REAGENT SETK821209 · CIQ | 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
