# Vistek Corp.

- Location (FDA's records): Santa Barbara, CA
- FDA decisions: 5 (1984–1990): 5 510(k) clearances
- Product codes: FWG (1), GEY (1), FTA (1), KQM (1), HBI (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
- K904682: Vistek Electronic Controller (Dec 18, 1990)
- K904681: VLS 5300 300W Xenon Light Source (Dec 18, 1990)
- K871034: LCA 2000 (Apr 10, 1987)
- K860173: Vis-2000 Video System (Feb 7, 1986)
- K843806: Vis-1000 Video System (Dec 12, 1984)

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