510(k) Report

FDA product code · Gastroenterology and urology

Colonic Irrigation System

KPLClass II21 CFR 876.5220510(k) required40 decisions since 19770 recalls

40 FDA decisions since 1977. 510(k) reviews decided 2021–2025 took a median of 604 days (half between 604 and 604). No recall names this code. The most-cited predicate is K131852, named by 3 later devices.

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 KPL 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 · KPL

1in 2022

2007: 12010: 12014: 12015: 12016: 12018: 12022: 1
2007high 1 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KPL

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

Recalls per year · KPL

No recall names KPL since 2007.

Adverse event reports per year · KPL

1in 2017

2007: 22010: 22013: 12017: 1
2007high 2 (2007) · low 0 (2008)2025

MAUDE reports naming product code KPL, 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—02
20080—00
20090—00
20101—02
20110—00
20120—00
20130—01
20141—00
20151—00
20161—00
20170—01
20181—00
20190—00
20200—00
20210—00
20221—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — KPL by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in KPL? 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 876.5220.