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 Diatech with 17 510(k) clearances. The most recent is a 510(k) clearance dated Aug 9, 1988: FIBRINOGENTEST-O.
| Date | Record | Source |
|---|---|---|
| Aug 9, 1988 | FIBRINOGENTEST-OK881685 · GIS | 510(k) clearances |
| Mar 12, 1986 | COASCREENER/DIASCREENERBLOOD PLASMA TIMING INST.K854938 · JPA | 510(k) clearances |
| Jan 6, 1986 | DIATIMER-1 BLOOD PLASMA CLOT TIMING INSTRUMENTK854089 · JPA | 510(k) clearances |
| Jan 6, 1986 | DIATIMER-2 BLOOD PLASMA CLOT TIMING INSTRUMENTK854090 · JPA | 510(k) clearances |
| Sep 11, 1984 | DIA T1, T2 & T3K842286 · JPK | 510(k) clearances |
| Jun 1, 1984 | DIA REPTINK841365 · GIR | 510(k) clearances |
| Jun 1, 1984 | HEPARIN COAGULATION CONTROL PLASMA 1-K841462 · JPA | 510(k) clearances |
| Jun 1, 1984 | DIA FIBRINK841366 · KQJ | 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
