# QLZ: Septostomy Catheter, Reprocessed

- Device class: 2; regulation: 21 CFR 870.5175; FDA's rule: 510(k) required
- FDA decisions: 2
- 510(k) review time 2021–2025: median 508 days (middle half 508–508)
- 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)
- 2020: 1
- 2023: 1

## Most-cited predicates
- K200060: Reprocessed NRG Transseptal Needle (2020), cited by 1

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