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 RIA Products with 9 510(k) clearances. The most recent is a 510(k) clearance dated Dec 17, 1981: NO-HOIL COMBOSTAT II KIT.
| Dec 17, 1981 | NO-HOIL COMBOSTAT II KITK813310 · CDD | 510(k) clearances |
| Jan 2, 1981 | CORTISOL 125-I RADIOIMMUNOASSAY KITK802969 · CGR | 510(k) clearances |
| Oct 23, 1980 | COMBOSTAT - NO-BOIL KITK801578 · CDD | 510(k) clearances |
| Oct 23, 1980 | VITAMIN B12 - NO-BOIL KITK801579 · CDD | 510(k) clearances |
| May 14, 1980 | FERRITIRON KIT CAT. #RP-1100K800710 · JQG | 510(k) clearances |
| May 8, 1980 | NO-BOIL FOLATE KIT #RP-500K800914 · CGN | 510(k) clearances |
| Jan 10, 1979 | FERRITIN KITK781844 · JMG | 510(k) clearances |
| Dec 4, 1978 | IRON 59 KITK781769 · JJA | 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
