510(k) Report

FDA product code · Gastroenterology and urology

Kit, Catheter, Urinary (Exludes Hiv Testing)

NWOClass II21 CFR 876.5130510(k) required1 decision since 20071 recall

1 FDA decision since 2007. 1 recall names this code; it is Class I. The most-cited predicate is K071496, named by 1 later device.

Urinary Catheterization Kit (Excludes HIV Testing)

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 NWO 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 · NWO

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NWO

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

Recalls per year · NWO

1in 2014

2014: 1, 1 Class I
2007high 1 (2014) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · NWO

1in 2023

2014: 12017: 22023: 1
2007high 2 (2017) · low 0 (2007)2025

MAUDE reports naming product code NWO, 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
20071—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—1 (1)1
20150—00
20160—00
20170—02
20180—00
20190—00
20200—00
20210—00
20220—00
20230—01
20240—00
20250—00
20260—0—
FIG. 1 — NWO by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NWO? 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

Related product codes

Other codes under 21 CFR 876.5130.