# LXS: Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

- Device class: 2; regulation: 21 CFR 886.4392; FDA's rule: 510(k) required
- FDA decisions: 7
- 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)
- 1984: 1
- 1985: 2
- 1986: 1
- 1989: 4
- 1990: 1
- 2002: 1

## Most-cited predicates
- K892058: ISL QC 2000 (1989), cited by 2
- K893987: Nidek Model YC-1200 (1989), cited by 1

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