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 Ria Diagnostics with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jan 24, 1986: T-3 UPTAKE/RIASSAY.
| Date | Record | Source |
|---|---|---|
| Jan 24, 1986 | T-3 UPTAKE/RIASSAYK855033 · KHQ | 510(k) clearances |
| Jan 15, 1986 | T-4 RIASSAYK854798 · CDX | 510(k) clearances |
| Aug 12, 1985 | T-3 RIASSAYK852537 · CDP | 510(k) clearances |
| Feb 19, 1981 | DIGOXIN RIA ASSAYK810296 · DON | 510(k) clearances |
| Aug 27, 1980 | TSH RIASSAYK801691 · JLW | 510(k) clearances |
| Feb 25, 1980 | THEOPHYLLINE RIASSAYK792062 · LCA | 510(k) clearances |
| Jan 20, 1978 | ANTITHROMBIN III RIAK780012 · DDQ | 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
