# Gesco Intl., Inc.

- Location (FDA's records): San Antonio, TX
- FDA decisions: 26 (1978–1995): 26 510(k) clearances
- Product codes: FOS (6), LJS (3), JOL (2), KNT (1), BSY (1), BSP (1), DYB (1), GBM (1), KNX (1), GBZ (1), FKO (1), MCY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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
- Reavillmed: 1 (https://510kreport.com/company/reavillmed)
- Neochild, LLC: 1 (https://510kreport.com/company/neochild)
- Promedic, Inc.: 1 (https://510kreport.com/company/promedic)
- Maquet Critical Care AB: 1 (https://510kreport.com/company/maquet-critical-care)

## Its most-cited devices
- K861090: Nutri-Cath - Feeding Tube (1986), cited by 2
- K940870: Umbili-Cath (1994), cited by 1
- K940871: Umbili-Cath-P (1994), cited by 1

## Recent decisions
- K954422: Per-Q-Cath Mid-Line (Dec 15, 1995)
- K940870: Umbili-Cath (Aug 2, 1994)
- K940953: Umbili-Cath-S (Aug 2, 1994)
- K940952: Umbili-Cath-S-DL (Jul 29, 1994)
- K941672: Uri-Cath Catheter (May 16, 1994)
- K941232: Thora-Cath (May 11, 1994)
- K940871: Umbili-Cath-P (Apr 29, 1994)
- K931989: Ventri-Cath (Jul 21, 1993)

Source page: https://510kreport.com/company/gesco-intl