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 Technia Diagnostics with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 10, 1986: AUTOFLUOR V.
| Date | Record | Source |
|---|---|---|
| Jun 10, 1986 | AUTOFLUOR VK861978 · KTL | 510(k) clearances |
| Sep 16, 1980 | T3(125) RADIOIMMUNOASSAY KITK801843 · CDP | 510(k) clearances |
| Jun 20, 1980 | DIGOXIN RADIOIMMUNOASSAY KITK801202 · LCS | 510(k) clearances |
| Jun 9, 1980 | CORTISOL RADIOIMMUNOASSAY KITK801203 · CGR | 510(k) clearances |
| Aug 16, 1979 | T3 UPTAKE RADIOIMMUNOASSAY KITK791361 · KHQ | 510(k) clearances |
| Jun 28, 1979 | HPL RIA KITK790919 · JMF | 510(k) clearances |
| May 3, 1979 | THYROXINE RIA KITK790495 · CDX | 510(k) clearances |
| Feb 28, 1979 | RIA KIT, VITAMIN B12K782024 · CDD | 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
