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 13, 2026, FDA's public records list Boots-Celltech Diagnostics with 20 510(k) clearances. The most recent is a 510(k) clearance dated Nov 17, 1989: IDEIA HERPES SIMPLEX VIRUS TEST.
| Date | Record | Source |
|---|---|---|
| Nov 17, 1989 | IDEIA HERPES SIMPLEX VIRUS TESTK871877 · LGC | 510(k) clearances |
| Dec 8, 1988 | MODIFIED IDEIA CHLAMYDIA TESTK880799 · LJC | 510(k) clearances |
| Apr 18, 1988 | SUCROSEP SPECIFIC IMMUNORADIOMETRIC ASSAYK880758 · CEP | 510(k) clearances |
| Mar 24, 1988 | CHEMELIA FREE THYROXINE(FT4)/ENZYME IMMUNO. (EIA)K874875 · CEC | 510(k) clearances |
| Feb 24, 1988 | IMAGEN INFLUENZA VIRUS A AND B TESTMIK872958 · GNX | 510(k) clearances |
| Feb 2, 1988 | OVEIA (TM) DUAL ANALYTEK872843 · JLP | 510(k) clearances |
| Oct 20, 1987 | CHEMELIA ENZYME IMMUNOASSAY FOR (TSH)K873625 · JLM | 510(k) clearances |
| Jun 15, 1987 | MODIFIED (DIRECTIONS FOR USE) FOR IDEIA(TM) TESTK872056 · LJC | 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
