Diagnostics 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 14, 2026, FDA's public records list Advanced Clinical Diagnostics with 19 510(k) clearances. The most recent is a 510(k) clearance dated Feb 3, 1994: TRANSFORMED PRIMARY HUMAN EMBRYONAL KIDNEY.
| Feb 3, 1994 | TRANSFORMED PRIMARY HUMAN EMBRYONAL KIDNEYK936171 · KIR | 510(k) clearances |
| Feb 3, 1994 | RHESUS MONKEY KIDNEY CELLS (LLC-MK2)K936172 · KIR | 510(k) clearances |
| Feb 3, 1994 | RHESUS MONKEY KIDNEY CELLSK936169 · KIR | 510(k) clearances |
| Jan 28, 1994 | RABBIT KIDNEY CELLS - R.K.C.K934934 · KIR | 510(k) clearances |
| Jan 28, 1994 | HELA-229/HELA CELLSK934973 · KIR | 510(k) clearances |
| Jan 24, 1994 | PRIMARY AFRICAN GREEN MONKEY KIDNEY CELLSK935766 · KIR | 510(k) clearances |
| Jan 3, 1994 | KIDNEY AFRICIAN GREEN MONKEY CELLS-VEROK934240 · KIR | 510(k) clearances |
| Jan 3, 1994 | CYNOMOLOGUS MONKEY KIDNEY CELLSK935336 · KIR | 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
