# SBO: Bed-Patient Activity Monitoring System

- Device class: 1; regulation: 21 CFR 880.2400; FDA's rule: 510(k) exempt
- FDA decisions: 1
- 510(k) review time 2021–2025: median 269 days (middle half 269–269)
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 2024: 1

## Most-cited predicates

Source page: https://510kreport.com/product-code/SBO
Data by year (CSV): https://510kreport.com/product-code/SBO.csv