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 Diagnostica, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Feb 23, 2001: EASE-A-CULT.
| Feb 23, 2001 | EASE-A-CULTK002756 · KHE | 510(k) clearances |
| Dec 28, 1982 | H. INFLUENZA B ANTISERA FOR CIEK823348 · GRP | 510(k) clearances |
| Sep 23, 1981 | DIAGNOSTIC KITS & KIT COMPONENTSK812434 · LHT | 510(k) clearances |
| Mar 12, 1980 | PARACONTROL ABNORMAL IMMUNOGLOBULIN CONTK800398 · DEW | 510(k) clearances |
| Nov 27, 1979 | ANTI-HUMAN IGG SERUMK791281 · DEW | 510(k) clearances |
| Nov 27, 1979 | ANTI-HUMAN LAMBDA SERUMK791283 · DEH | 510(k) clearances |
| Nov 27, 1979 | ANTI-HUMAN KAPPA SERUMK791284 · DFH | 510(k) clearances |
| Oct 17, 1979 | ANTI-HUMAN SERUMK791282 · DGQ | 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
