510(k) Report

510(k) · Cleared

Cleared

Nexus Irrigation Tubing Set

K062551510(k) TraditionalCleared Dec 15, 2006107-day reviewClass II21 CFR 876.5130

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

Nexus Medical, LLC · LJH System, Irrigation, Urological

Cleared on Dec 15, 2006 after a 107-day review. FDA’s file for it is a 510(k) statement, which names no predicate.

Decided
Dec 15, 2006
Review
107 days
Class
Class II
Product code
LJH
Recalls
None
Predicates
0

FDA’s file for it is a 510(k) statement, which names no predicate.

FIG. 1 — Lineage of K062551Source: FDA 510(k) database · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LJH? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new LJH device

  1. #1 K254111 Irrigation/Urology Setsscore 12.0 · 1 generation · no Class I recall
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What was it cleared against?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

How does its category compare?

All LJH devices

LJH System, Irrigation, Urological: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LJH

1in 2017

2007: 32017: 12026 (partial year): 2
2007high 3 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LJH

77in 2007

2007: 77 days median
2007high 77 (2007)2026

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

Recalls per year · LJH

1in 2022

2022: 1
2007high 1 (2022) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LJH

25in 2025

2008: 12010: 302011: 272012: 222013: 442014: 972015: 6422016: 322017: 192018: 182019: 162020: 232021: 152022: 212023: 342024: 132025: 25
2007high 642 (2015) · low 0 (2007)2025

MAUDE reports naming product code LJH, 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
200737700
20080—01
20090—00
20100—030
20110—027
20120—022
20130—044
20140—097
20150—0642
20160—032
20171—019
20180—018
20190—016
20200—023
20210—015
20220—121
20230—034
20240—013
20250—025
20262—0—

What is it indicated for?

The Nexus Irrigation Tubing Set is intended for delivery of irrigatirng solutions from a container to an irrigation site during bladder irrigation, or endoscopic procedures such as cystoscopy, transurethral resection (TUR) and arthroscopic prqcedures.

Indications for use as stated in the FDA 510(k) statement.

Cite this page

510(k) Report. “K062551: Nexus Irrigation Tubing Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K062551

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026