Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Agilent TechnologiesLabelled 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 14, 2026, FDA's public records list Dako Diagnostics with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 28, 1998: IMAGEARAINFLUENZA VIRUS GROUP (TYPES 1,2 AND 3) TEST AND IMAGEN PARAINFLUENZA VIRUS TEST….
| Sep 28, 1998 | IMAGEARAINFLUENZA VIRUS GROUP (TYPES 1,2 AND 3) TEST AND IMAGEN PARAINFLUENZA VIRUS TEST TYPES 1,2 AND 3K981226 · GQP | 510(k) clearances |
| Dec 22, 1997 | IMAGEN RESPIRATORY SCREENK973954 · GNW | 510(k) clearances |
| Dec 26, 1996 | IMAGEN RESPIRATORY SCREENK962037 · GNW | 510(k) clearances |
| Jan 11, 1996 | IDEIA(TM) CHLAMYDIA BLOCKING REAGENTS, MODIFICATIONK940564 · LJC | 510(k) clearances |
| Jan 9, 1995 | IMAGENK943557 · GQS | 510(k) clearances |
| Dec 27, 1993 | IDEIA(TM) ROTAVIRUSK932384 · LIQ | 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
