# Zeus Technologies

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1983–1988): 4 510(k) clearances and 1 original PMA approval
- Product codes: LHL (2), JWX (1), GRZ (1), LPJ (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
- P860015: Fluoro-Cep{R} Estrogen Assay Reagent (Feb 29, 1988)
- K840012: Indirect Fluorescent Antibody Myco (Feb 27, 1984)
- K831026: Indirect Fluorescent Antibody Reagents (Jun 22, 1983)
- K830783: Veri-Staph (Apr 8, 1983)
- K822859: Direct FA Conjugate for Legionella SPP (Feb 16, 1983)

Source page: https://510kreport.com/company/zeus-technologies