Pharmaceutical companyLabelled 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 PfizerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record. See the Pfizer group view.
As of Nov 14, 2026, FDA's public records list G.D. Searle with 56 510(k) clearances and 30 drug applications. The most recent is a 510(k) clearance dated May 25, 1982: IN-LINE OXYGEN MONITORING SYSTEM.
| May 25, 1982 | IN-LINE OXYGEN MONITORING SYSTEMK821159 · DRY | 510(k) clearances |
| May 27, 1981 | BYPASS COILK811068 · KPY | 510(k) clearances |
| May 5, 1981 | VENOUS OXYGEN PROBEK811071 · CCE | 510(k) clearances |
| Apr 23, 1981 | INTRAVASCULAR CATHETERK803238 · FOZ | 510(k) clearances |
| Mar 31, 1981 | SILICONE ELASTOMER COATED LATEX FOLEYK810630 · KOD | 510(k) clearances |
| Feb 26, 1981 | ADMINISTRATION SETK810131 · FPD | 510(k) clearances |
| Feb 12, 1981 | SEARLE VASCULAR LOOPSK802485 · KDC | 510(k) clearances |
| Feb 10, 1981 | METRONIDAZOLE DISCSK801805 · JWY | 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
