# Siegen Corp.

- Location (FDA's records): Mountain View, CA
- FDA decisions: 6 (1984–1987): 6 510(k) clearances
- Product codes: GWF (2), GXY (1), GWO (1), GWE (1), GWJ (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
- K871964: Siegen Neuroscope Seeg for Evoked Response Stimu. (Oct 1, 1987)
- K861884: Neuroscope Seeg (Oct 14, 1986)
- K862430: Siegen Headphones (Sep 26, 1986)
- K844616: Siegen Visual Stimulator (Feb 14, 1985)
- K844646: Siegen Surface Electrodes (Dec 11, 1984)
- K843464: Siegen Neuroscope (Nov 20, 1984)

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