# Seragen Diagnostics, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 20 (1982–1987): 20 510(k) clearances
- Product codes: JJT (2), GKL (2), JGS (1), CKG (1), GRP (1), JIW (1), CDQ (1), LJC (1), CEX (1), LKJ (1), CGA (1), GIF (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
- K872148: Vivid Chlamydia (TM) (Aug 19, 1987)
- K851663: Quick-Count Hematology Controls (Jul 23, 1985)
- K852260: Quick-Chem Calibration Set (Jul 22, 1985)
- K851520: CK/LD Isoenzymes Controls (Human) (Jun 25, 1985)
- K851521: LD-1(Immuno) Separation Set (May 10, 1985)
- K850209: Quick-Lyte (Feb 27, 1985)
- K844743: Seratest Ena (RNP/SM) Determination (Feb 4, 1985)
- K842563: Seratest Dna Determination (Oct 25, 1984)

Source page: https://510kreport.com/company/seragen-diagnostics