# PMU: Containment System, Laparoscopic Power Morcellation, With Instrument Port

- Device class: 2; regulation: 21 CFR 884.4050; FDA's rule: 510(k) required
- FDA decisions: 4
- 510(k) review time 2021–2025: median 80 days (middle half 80–81)
- 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)
- 2016: 1
- 2020: 1
- 2021: 1
- 2025: 1

## Most-cited predicates
- K192898: PneumoLiner (2020), cited by 2
- DEN150028: PneumoLiner (2016), cited by 1

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