# Lasertek OY

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1979–1984): 4 510(k) clearances
- Product codes: HQF (3)
- 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
- K832089: Model 150K Laser Coagulator (Jan 30, 1984)
- K828326: Unknown (Mar 4, 1983)
- K781965: Laser Coagulator, Model 41AK (Feb 8, 1979)
- K782106: Coagulator, Model 40 Aargon (Feb 8, 1979)

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