# Lasag AG

- Location (FDA's records): Eden Prairie, MN
- FDA decisions: 2 (1989–1990): 2 510(k) clearances
- Product codes: LXS (1), HQF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K900199: Lasag Microrupter 2 ND:Yag Laser Trabeculoplasty (Mar 27, 1990)
- K895864: Microruptor Iii Syst, Q-Switched ND:Yag Laser Comp (Dec 29, 1989)

Source page: https://510kreport.com/company/lasag