# Automated Screening Devices

- Location (FDA's records): Mchenry, IL
- FDA decisions: 2 (1978–1980): 2 510(k) clearances
- Product codes: DXN (2)
- 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
- K792653: Sentry (Jan 4, 1980)
- K782000: Monitor, Non-Invasive Blood Pressure (Dec 5, 1978)

Source page: https://510kreport.com/company/automated-screening-devices