# Ab Medett Produkter

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1979–1979): 3 510(k) clearances
- Product codes: KNX (2), KNK (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
- K791198: BIBAG (Jul 30, 1979)
- K791197: Uridrop Special (Jul 30, 1979)
- K791196: Uridrop (Jul 30, 1979)

Source page: https://510kreport.com/company/ab-medett-produkter