# Laserguide

- Location (FDA's records): Santa Barbara, CA
- FDA decisions: 5 (1987–1988): 5 510(k) clearances
- Product codes: GEX (2), LNK (1), LLO (1), FCS (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
- K880071: Surgi-Light ND:Yag Laser for Urological Use (Mar 22, 1988)
- K873892: Surgi-Light Dispos.Fiberoptic Del/Sys GI/Uro Use (Feb 2, 1988)
- K875104: Surgi-Light Disposable System for Pulmonology Use (Feb 2, 1988)
- K873571: Light-Touch Fiberoptic Microcontact Probe (Nov 6, 1987)
- K873664: Light-Spot Fiberoptic Laser Handpiece (Nov 6, 1987)

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