# Vicon Instrument Co.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1976–1981): 8 510(k) clearances
- Product codes: ESD (4), KLW (2), EWO (1), ETS (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
- K811751: Finetone Model VI Hearing Aid (Jul 15, 1981)
- K790878: Screening Audiometer, High Frequency (Aug 3, 1979)
- K790064: Tinnitus Devices (Feb 16, 1979)
- K771769: Tinnitus Maskers, Models S564&S574 (Jan 3, 1978)
- K771762: Modular Hearing Device, Model S291 (Oct 4, 1977)
- K770938: Tinnitus Aid, Model S244 (Jun 28, 1977)
- K761216: Hearing Aids (Model E-552 S-712) (Dec 16, 1976)
- K760215: Hearing Aid, S-522 FM (Jul 21, 1976)

Source page: https://510kreport.com/company/vicon-instrument