# K930483: Ureteral Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Surgitek
- Decided: Jul 16, 1993 after 168 days
- Product code: EYB (Catheter, Ureteral, Gastro-Urology)
- Device class: 2
- Regulation: 21 CFR 876.5130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K043581: Dual Lumen Catheter (2005), 1 descendant of its own
- K180182: Dual Lumen Ureteral Access Catheter, Flexi-Tip Dual Lumen Ureteral Access Catheter (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K930483
Methodology: https://510kreport.com/methodology