# LOQ: Device, General Purpose, Hematology

- Device class: 2; regulation: 21 CFR 866.6010; FDA's rule: 510(k) required
- FDA decisions: 1
- Recalls: 1 (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

## Most-cited predicates
- K981592: Acs:Centaur Afp (1998), cited by 1

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