# Atrix

- Location (FDA's records): Portland, OR
- FDA decisions: 2 (1985–1986): 2 510(k) clearances
- Product codes: LOS (1), DPS (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
- K852829: Cardisuny 501 a (Feb 26, 1986)
- K842759: Model 503FB (Jan 18, 1985)

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