510(k) Report

FDA product code · Gastroenterology and urology

Gallbladder Drainage Stent And Delivery System

QXHClass II21 CFR 876.5016510(k) required1 decision since 20230 recalls

1 FDA decision since 2023. No recall names this code. The most-cited predicate is DEN230019, named by 2 later devices.

A gallbladder drainage stent is a prescription device intended to facilitate transgastric or transduodenal endoscopic drainage of the gallbladder. This device may also include a delivery system.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, gastroenterology and urology panel

Twenty years of QXH at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · QXH

1in 2023

2023: 1
2007high 1 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QXH

Too few QXH 510(k)s in any year since 2007 to give a median.

Recalls per year · QXH

No recall names QXH since 2007.

Adverse event reports per year · QXH

45in 2025

2025: 45
2007high 45 (2025) · low 0 (2007)2025

MAUDE reports naming product code QXH, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20231—00
20240—00
20250—045
20260—0—
FIG. 1 — QXH by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in QXH? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report