# Kmb Medical Products Co.

- Location (FDA's records): Hazelwood, MO
- FDA decisions: 1 (1988–1988): 1 510(k) clearance
- Product codes: FEG (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: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K880850: Keith Nasogastric Sump Tube W/Anti-Reflux Valve (May 26, 1988)

Source page: https://510kreport.com/company/kmb-medical-products