Medical device 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 13, 2026, FDA's public records list Cytotech, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Aug 4, 1988: CIRCULATING IMMUNE COMPLEXES CONTROLS.
| Date | Record | Source |
|---|---|---|
| Aug 4, 1988 | CIRCULATING IMMUNE COMPLEXES CONTROLSK882829 · DAK | 510(k) clearances |
| Nov 25, 1987 | CIC-RAJI CELL REPLACEMENT ENZYME IMMUNOASSAYK874379 · CZY | 510(k) clearances |
| Sep 22, 1987 | ANTINUCLEAR ANTIBODY (ANA) POSITIVE CONTROLSK873249 · LKJ | 510(k) clearances |
| Jul 23, 1987 | CYTOTECH C1-INHIBITOR ENZYME IMMUNOASSAYK872426 · DBA | 510(k) clearances |
| Jun 9, 1987 | CYTOTECH ANTINUCLEAR ANTIBODY (ANA) IFA KITK871801 · DHN | 510(k) clearances |
| Feb 2, 1987 | CYTOTECH RUBELLA IGG ENZYME IMMUNOASSAYK864315 · LFX | 510(k) clearances |
| Dec 9, 1986 | CYTOTECH HSV IGG ENZYME IMMUNOASSAYK862838 · GCO | 510(k) clearances |
| Nov 13, 1986 | CYTOTECH TOXOPLASMA IGG ENZYME IMMUNOASSAYK863363 · LGD | 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
