# Minnesota Laser Corp.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 12 (1985–1988): 12 510(k) clearances
- Product codes: GEX (5), HHR (2), LNK (2), EWG (2), LLO (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
- K874255: ND:Yag Surgical Laser for Endo. Gastro/Uro. Appli. (Jul 12, 1988)
- K874253: ND:Yag Surgical Laser for Gastro/Urology Applica. (Jul 12, 1988)
- K874254: ND:Yag Surgical Laser for Pulmonary Applications (Mar 4, 1988)
- K854468: Portalase 200 Carbon Dioxide Surg Laser Neurologic (Jun 20, 1986)
- K854473: Portalase 300 Carbon Dioxide Surg Laser Neurologic (Jun 20, 1986)
- K854471: Portalase 300 Carbon Dioxide Surg Laser Ear/Nose/T (Feb 13, 1986)
- K854469: Portalase 200 Carbon Dioxide Surg Laser Dermatolog (Feb 11, 1986)
- K854472: Portalase 300 Carbon Dioxide Surg Laser Dermatolog (Feb 11, 1986)

Source page: https://510kreport.com/company/minnesota-laser