# SEM: Sub-Scalp Implanted Electroencephalogram System For Remote Patient Monitoring

- Device class: 2; regulation: 21 CFR 882.1360; FDA's rule: 510(k) required
- FDA decisions: 2
- 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)
- 2025: 1
- 2026: 1

## Most-cited predicates
- DEN240062: Minder System (2025), cited by 1

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