# Western Advanced Technology, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1980–1983): 6 510(k) clearances
- Product codes: ETS (3), GZJ (1), ESD (1), EIB (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
- K822411: System 80 Faceplate-in-the-Ear #F1 (Jul 12, 1983)
- K813557: Auditory Stimulator (Jan 19, 1982)
- K812138: Tens Device (Aug 20, 1981)
- K811772: Auditory Localizer (Jul 15, 1981)
- K811790: Octotoxic Screener (Jul 15, 1981)
- K802324: E1 Series Hearing Aid (Oct 10, 1980)

Source page: https://510kreport.com/company/western-advanced-technology