# Norwich Eaton Pharmaceuticals, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 10 (1980–1984): 10 510(k) clearances
- Product codes: KNT (9), KHT (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
- K842841: Vivonex Tung Sten Tip Tube (Aug 14, 1984)
- K831968: Vivonex Tungsten Tip Tube-Braided (Sep 1, 1983)
- K831969: Vivonex Tungsten Tip Tube-Wound (Sep 1, 1983)
- K831971: Vivonex Tungsten Tip Tube-Twisted Wire (Sep 1, 1983)
- K831970: Vivonex Tungsten Tip Tube-Monofila- (Jul 18, 1983)
- K822516: Vivonex Mass Gastrastomy Tube (Sep 7, 1982)
- K821231: Vivonex Tungsten Tip Tube Placement (May 10, 1982)
- K821067: Vivonex Acutrol Enternal Feeding Sys (Apr 29, 1982)

Source page: https://510kreport.com/company/norwich-eaton-pharmaceuticals