Diagnostics makerLabelled 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.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Livonia Diagnostics with 16 510(k) clearances. The most recent is a 510(k) clearance dated Jun 10, 1985: SERUM IRON/VIBC REAGENT SET.
| Jun 10, 1985 | SERUM IRON/VIBC REAGENT SETK852161 · JIY | 510(k) clearances |
| Nov 27, 1984 | SGPT REAGENT SETK844283 · CKD | 510(k) clearances |
| Nov 27, 1984 | SGOT REAGENT SETK844322 · CIQ | 510(k) clearances |
| Nov 20, 1984 | ALKALINE PHOSPHATASE REAGENT SETK844237 · CIO | 510(k) clearances |
| Nov 13, 1984 | UREA NITROGEN REAGENT SETK844156 · CDW | 510(k) clearances |
| Nov 9, 1984 | INORGANIC PHOSPHORUS REAGENT SETK844182 · CEO | 510(k) clearances |
| Nov 2, 1984 | HDL PRECIPATATING REAGENT SETK843894 · LBR | 510(k) clearances |
| Oct 30, 1984 | CREATININE REAGENT SETK844024 · CGX | 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
