# Eswallow USA

- Location (FDA's records): Guntersville, AL
- FDA decisions: 2 (2011–2013): 2 510(k) clearances
- Product codes: GXY (1), IPF (1)
- Predicates its devices cite: 2 (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

## Firms whose devices it cites most
- Selectivemed Components, Inc.: 1 (https://510kreport.com/company/selectivemed-components)
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)

## Recent decisions
- K113375: Eswallow Usa Electrode,Eswallow Usa Leadwire (Jan 25, 2013)
- K092202: Eswallow Dysphagia Therapy Kit, Pmi Dysphagia Therapy Kit (Feb 10, 2011)

Source page: https://510kreport.com/company/eswallow-usa