# K032521: Bard Dual Lumen Ureteral Catheter

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Nov 14, 2003 after 91 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Bard Dual Lumen Ureteral Catheter: named in the summary without a submission number

## Most influential descendants
- K083788: Endo Optiks Urological Catheter for Endoscopy, Model Sessr (2009), 0 descendants of its own

## Indications for use
The Bard@Dual Lumen Ureteral Catheter is intended to facilitate drainage and retrograde pyelogram of the upper urinary tract. This catheter will allow access to and navigation of a torturous ureter using standard endoscopic techniques.

Source page: https://510kreport.com/device/K032521
Methodology: https://510kreport.com/methodology