# Damon Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 11 (1976–1987): 11 510(k) clearances
- Product codes: JQC (2), LLZ (1), CDZ (1), CKG (1), DON (1), CDP (1), CEC (1), JLS (1), JPA (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K874865: Damon D.E.T.E.C.T Image Enhancer (Dec 23, 1987)
- K831826: Adrenocorticotropin Radio-Immunoassay (Jul 18, 1983)
- K820686: Liquisol Progesterone Radioimmuno (Apr 1, 1982)
- K802661: Liquisol Testosterone Radioimm. Test Kit (Dec 10, 1980)
- K790250: Liquisol Cortisol Ria Test Kit (Apr 4, 1979)
- K782124: Iec Centra-7 Centrifuge Model 2362 (Feb 26, 1979)
- K781012: Ria Test Kit Sys. Damon Kiquisol Free (Jul 27, 1978)
- K780207: Liquisol Digoxin Ria Test Kit (Feb 23, 1978)

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