# LRL: Cushion, Hemorrhoid

- Device class: U; regulation: 21 CFR —
- FDA decisions: 3
- 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)
- 1987: 1
- 1993: 1
- 2007: 1

## Most-cited predicates
- K864470: Hemorest (TM) (1987), cited by 1

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