# KGL: Cabinet, Phototherapy (Puva)

- Device class: 2; regulation: 21 CFR 878.4630; FDA's rule: 510(k) required
- FDA decisions: 8
- 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)
- 1976: 1
- 1979: 2
- 1981: 2
- 1982: 1
- 1984: 1
- 1985: 1

## Most-cited predicates
- K841795: UV 8001K, Puva 800, Puva 180/200 1000 (1984), cited by 1

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