# LGN: Chamber, Patient Transport Isolation

- Device class: 2; regulation: 21 CFR 880.5450; 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)
- 1979: 1
- 2006: 1

## Most-cited predicates
- K052798: Capsuls, Models 2003-PUR8C, 2004-PVC8C (2006), cited by 2

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