# Lake Medical Products, Inc.

- Location (FDA's records): Maryland Heights, MO
- FDA decisions: 15 (1987–1995): 15 510(k) clearances
- Product codes: KNT (3), KOD (2), FCN (1), CBT (1), EXB (1), LRO (1), FCM (1), FLL (1), FNM (1), KGC (1), FMI (1), IOQ (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
- K943162: Lake Stagezero (TM) Air Flotation Bed (Feb 27, 1995)
- K922730: Lake Ostomy Care Set (Dec 30, 1993)
- K905053: Stage Zero Air Flotation Bed (Nov 26, 1990)
- K901835: Lake N/G Feeding Tube (with Y Port Connector) (Sep 5, 1990)
- K902508: Lake Male External Catheterization Kit (Aug 23, 1990)
- K902121: Lake Gastrostomy Tube (Jul 27, 1990)
- K884127: Lake N/G Feeding Tube (Feb 8, 1989)
- K884128: Lake N/G Extension Set (Dec 8, 1988)

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