# MOQ: Battery, Replacement, Rechargeable

- Device class: 1; regulation: 21 CFR 878.4820; FDA's rule: 510(k) exempt
- FDA decisions: 3
- Recalls: 2 (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)
- 1998: 1
- 2001: 1
- 2008: 1

## Most-cited predicates
- K081713: Vertebral Access System by Vidacare (2008), cited by 1

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