# Cytotech, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 10 (1986–1988): 10 510(k) clearances
- Product codes: DAK (2), LKJ (1), DBA (1), GQI (1), GCO (1), LFX (1), DHN (1), CZY (1), LGD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K882829: Circulating Immune Complexes Controls (Aug 4, 1988)
- K874379: Cic-Raji Cell Replacement Enzyme Immunoassay (Nov 25, 1987)
- K873249: Antinuclear Antibody (Ana) Positive Controls (Sep 22, 1987)
- K872426: Cytotech C1-Inhibitor Enzyme Immunoassay (Jul 23, 1987)
- K871801: Cytotech Antinuclear Antibody (Ana) Ifa Kit (Jun 9, 1987)
- K864315: Cytotech Rubella Igg Enzyme Immunoassay (Feb 2, 1987)
- K862838: Cytotech HSV Igg Enzyme Immunoassay (Dec 9, 1986)
- K863363: Cytotech Toxoplasma Igg Enzyme Immunoassay (Nov 13, 1986)

Source page: https://510kreport.com/company/cytotech