# PKA: External Upper Esophageal Sphincter (Ues) Compression Device

- Device class: 2; regulation: 21 CFR 874.5900; FDA's rule: 510(k) required
- FDA decisions: 2
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 2015: 1
- 2018: 1

## Most-cited predicates
- DEN130046: Reza Band (TM) Upper Esophageal (Ues) Sphincter Assist Device (2015), cited by 1

Source page: https://510kreport.com/product-code/PKA
Data by year (CSV): https://510kreport.com/product-code/PKA.csv