# Dytek Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1976–1978): 3 510(k) clearances
- Product codes: BWF (2), GEI (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
- K781245: Lung Exer. Bag, Post-OP, Modified (Sep 20, 1978)
- K760168: Pencil, Electrosurgical (Aug 9, 1976)
- K760167: Bag, Post Operative Lung Exercizing Blow (Aug 6, 1976)

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