# PQY: Nonthermal Shortwave Therapy Device Indicated For Over The Counter Use For The Treatment Of Pain

- Device class: 2; regulation: 21 CFR 890.5290; 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)
- 2017: 1
- 2020: 1

## Most-cited predicates
- K152432: ActiPatch (R) (2017), cited by 1

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