# Neal & Assoc., Inc.

- Location (FDA's records): Columbia, MO
- FDA decisions: 2 (1988–1993): 2 510(k) clearances
- Product codes: LDF (1), FMQ (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
- K925924: Neal Wrist Cones (Apr 8, 1993)
- K881356: External Pacemaker Wire Dressing Change (May 19, 1988)

Source page: https://510kreport.com/company/neal-assoc