# Viggo Products

- Location (FDA's records): Madison, WI
- FDA decisions: 7 (1985–1985): 7 510(k) clearances
- Product codes: FOZ (4), FPA (2), FMG (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
- K850769: Viggo Accessories for I.V. Therapy (May 29, 1985)
- K850277: Viggo I.V. Accessories-Viggo Extension Tubes Etc. (Apr 12, 1985)
- K850276: Viggo Neoflon Infusion Cannula (Apr 12, 1985)
- K850280: Viggo Connecta 3-Way Infusion Stopcock (Apr 11, 1985)
- K850460: Viggo Secalon T Catheter (Apr 11, 1985)
- K850278: Vasculon I.V. Cannulae (Apr 9, 1985)
- K850349: Viggo Arterial Cannula (Apr 9, 1985)

Source page: https://510kreport.com/company/viggo-products