# Wako Intl., Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1978–1979): 4 510(k) clearances
- Product codes: CGA (1), CHH (1), JKA (1), CDL (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
- K790768: Wako Cholesterol Test (May 23, 1979)
- K781899: Urea Nitrogen Test (Dec 20, 1978)
- K781629: Seri-Sep Serum/Plasma Islolator (Oct 27, 1978)
- K781342: Glucose Test (Aug 31, 1978)

Source page: https://510kreport.com/company/wako-intl