# Akron Catheter, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1976–1986): 3 510(k) clearances
- Product codes: KOD (2), FGE (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
- K864736: Akro-Sil Plus (Dec 24, 1986)
- K823428: Kelly Inflatable T Drain (Jan 18, 1983)
- K760440: Catheter, Natural Latex Urethral (Oct 20, 1976)

Source page: https://510kreport.com/company/akron-catheter