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 Oxford Laboratories with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 28, 1978: ADJUSTABLE DISPENSOR.
| Jun 28, 1978 | ADJUSTABLE DISPENSORK780912 · JQW | 510(k) clearances |
| Jul 20, 1976 | SERUM, B1A GLOBULIN C3C GOAT ANTI-HUMANK760148 · CZW | 510(k) clearances |
| Jul 20, 1976 | REAGENT, THYROXINE T4 (#210)K760079 · CDX | 510(k) clearances |
| Jul 20, 1976 | SERUM, HAPTOGLOBIN GOAT ANTI-HUMAN ACIDK760144 · DAD | 510(k) clearances |
| Jul 20, 1976 | SERUM, IGA GOAT ANTI-HUMAN ACIDK760146 · CZP | 510(k) clearances |
| Jul 20, 1976 | REAGENT, RIA TRIIODOTHYRONINE T3 (#200)K760078 · CDP | 510(k) clearances |
| Jul 20, 1976 | SERUM, ALPHA-1-GLYCOPROTEIN ANTI-HUMANK760143 · DEX | 510(k) clearances |
| Jul 20, 1976 | SERUM, IGM ANTI-HUMAN ACIDK760147 · DFT | 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
