# LPQ: Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

- Device class: 2; regulation: 21 CFR 890.5870; FDA's rule: 510(k) required
- FDA decisions: 0
- Recalls: 2 (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)
- 2004: 2
- 2005: 1
- 2006: 3
- 2007: 3
- 2008: 2
- 2009: 2
- 2010: 1
- 2012: 1
- 2014: 4
- 2015: 1

## Most-cited predicates

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