# DWQ: Stripper, Vein, External

- Device class: 2; regulation: 21 CFR 870.4885; FDA's rule: 510(k) required
- FDA decisions: 8
- 510(k) review time 2021–2025: median 202 days (middle half 202–202)
- Recalls: 1 (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)
- 1981: 1
- 1987: 1
- 1990: 1
- 1991: 2
- 2003: 1
- 2004: 1
- 2022: 1

## Most-cited predicates
- K032387: Trivex System (2003), cited by 1

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