# Endotronics, Inc.

- Location (FDA's records): Coon Rapids, MN
- FDA decisions: 3 (1986–1988): 3 510(k) clearances
- Product codes: KJH (3)
- 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
- K875151: Acusyst-P/3X (Jan 12, 1988)
- K872086: Acusyst-JR (Jun 15, 1987)
- K864334: Acusyst-P (Cell Culture Equipment) (Nov 24, 1986)

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