510(k) Report

FDA product code · Gastroenterology and urology

Gastrointesinal Lesion Software Detection System

QNPClass II21 CFR 876.1520510(k) required23 decisions since 20210 recalls

23 FDA decisions since 2021. 510(k) reviews decided 2021–2025 took a median of 30 days (half between 28 and 201). No recall names this code. The most-cited predicate is DEN200055, named by 5 later devices.

A gastrointestinal lesion software detection system is a computer-assisted detection device used in conjunction with endoscopy for the detection of abnormal lesions in the gastrointestinal tract. This device with advanced software algorithms brings attention to images to aid in the detection of lesions. The device may contain hardware to support interfacing with an endoscope.

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 QNP 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 · QNP

5in 2025

2021: 32022: 12023: 42024: 52025: 52026 (partial year): 5
2007high 5 (2024) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QNP

28in 2025

2023: 140 days median2024: 29 days median2025: 28 days median2026 (partial year): 169 days median
2007high 169 (2026) · low 28 (2025)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · QNP

No recall names QNP since 2007.

Adverse event reports per year · QNP

1in 2024

2024: 1
2007high 1 (2024) · low 0 (2007)2025

MAUDE reports naming product code QNP, 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
20213—00
20221—00
2023414000
202452901
202552800
202651690—
FIG. 1 — QNP by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in QNP? 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