# PCV: Endoscopic Leak Tester

- Device class: 2; regulation: 21 CFR 876.1500; FDA's rule: 510(k) required
- FDA decisions: 2
- 510(k) review time 2021–2025: median 79 days (middle half 79–79)
- 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)
- 2013: 1
- 2021: 1

## Most-cited predicates
- K123704: Automated Endoscope Leak Tester (2013), cited by 1

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