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 15, 2026, FDA's public records list Radioimmunoassay with 9 510(k) clearances. The most recent is a 510(k) clearance dated Oct 10, 1980: TESTOSTERONE RADIOIMMUNOASSY KIT.
| Oct 10, 1980 | TESTOSTERONE RADIOIMMUNOASSY KITK802135 · CDZ | 510(k) clearances |
| Feb 13, 1980 | LUTEINIZING HORMONE RADIOIMMUNOASSAY SYSK800106 · CEP | 510(k) clearances |
| Feb 13, 1980 | FOLLICLE STIMULATING HORMONEK800107 · CGJ | 510(k) clearances |
| Jan 16, 1980 | TRIIODOTHYRONINE RIA SYSTEMK792539 · CDP | 510(k) clearances |
| Nov 13, 1979 | THYROID STIMULATING HORMONEK792154 · JLW | 510(k) clearances |
| Nov 13, 1979 | DIGOXIN RADIOIMMUNOASSAY SYSTEMK792153 · DPB | 510(k) clearances |
| Oct 30, 1979 | CORTISOL RADIOIMMUNOASSAY SYSTEMK792036 · CGR | 510(k) clearances |
| Jun 6, 1978 | 125 I-T3 UPTAKE REAGENTK780671 · CEE | 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
