# Eyetech, LLC

- Location (FDA's records): Chicago, IL
- FDA decisions: 2 (1984–1990): 1 510(k) clearance and 1 original PMA approval
- Product codes: HKX (1), HQL (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
- P880082: Model 14760 UV Absorbing Posterior Chamber Lenses (Jun 13, 1990)
- K843354: Episcleral Venous Pressure (Nov 19, 1984)

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