# Douglas Bueschel

- Location (FDA's records): Santa Barbara, CA
- FDA decisions: 1 (1996–1996): 1 510(k) clearance
- Product codes: FTL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Minnesota Medical Development, Inc.: 1 (https://510kreport.com/company/minnesota-medical-development)

## Its most-cited devices
- K963141: Kugel Hernia Patch (1996), cited by 2

## Recent decisions
- K963141: Kugel Hernia Patch (Oct 11, 1996)

Source page: https://510kreport.com/company/douglas-bueschel