# Eschmann Bros. & Walsh, Ltd.

- Location (FDA's records): Sussex  Bn15 8tj, GB
- FDA decisions: 3 (1978–1987): 3 510(k) clearances
- Product codes: GEI (1), HHW (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
- K864637: Modified Eschmann Dilatation Catheter (Jan 6, 1987)
- K852935: Eschmann Electrosurgical Unit, Model TD411 (Oct 10, 1985)
- K781863: Device, Female Incontinence (Nov 6, 1978)

Source page: https://510kreport.com/company/eschmann-bros-walsh