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 14, 2026, FDA's public records list Connecticut Diagnostics, Ltd. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Mar 29, 1991: VISI-STAPH.
| Mar 29, 1991 | VISI-STAPHK905617 · JWX | 510(k) clearances |
| Sep 17, 1982 | CDL ISOTONIC DILUENTK822501 · GIF | 510(k) clearances |
| Sep 17, 1982 | CDL LYSING REAGENTK822500 · GGK | 510(k) clearances |
| Sep 17, 1982 | CDL AUTO-LYSING REAGENTK822504 · GGK | 510(k) clearances |
| May 21, 1981 | INORGANIC PHOSPHORUS REAGENTSK811222 · CED | 510(k) clearances |
| Oct 10, 1980 | GLUCOSE DIAGNOSTIC REAGENTK801897 · CGA | 510(k) clearances |
| Oct 10, 1980 | URIC ACID DIAGNOSTIC REAGENTK801898 · KNK | 510(k) clearances |
| Dec 18, 1979 | CONNECTICUT DIAGNOSTICS, LTS. DIRECTK792465 · CIG | 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
