Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 IDT, a division of Whittaker M.A. Bioproducts with 5 510(k) clearances. The most recent is a 510(k) clearance dated Feb 4, 1986: FIAX TEST KIT FOR VARICELLA ANTIBODY SEROLOGY.
| Date | Record | Source |
|---|---|---|
| Feb 4, 1986 | FIAX TEST KIT FOR VARICELLA ANTIBODY SEROLOGYK853540 · GQX | 510(k) clearances |
| Oct 22, 1985 | FIAX TEST KIT FOR MEASLES-G ANTIBODIES FLYORESCENTK853067 · GRE | 510(k) clearances |
| Jan 3, 1979 | FIAX TEST KITK782041 · DHN | 510(k) clearances |
| Jan 20, 1978 | FIAX TEST FOR ANTI-RUBELLA ANTIBODYK772219 · DHN | 510(k) clearances |
| Nov 30, 1977 | FIAX C4 ASSAYK772114 · DAK | 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
