510(k) Report

510(k) · Cleared

Cleared

Irrigation/Urology Sets

K254111510(k) TraditionalCleared Sep 10, 2026265-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

B.Braun Medical, Inc. · LJH System, Irrigation, Urological

Cleared on Sep 10, 2026 as substantially equivalent to K960787 (Baxter Healthcare Corp, 1996) after a 265-day review. Its family tree reaches back 1 generation to 1996.

Decided
Sep 10, 2026
Review
265 days
Class
Class II
Product code
LJH
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K960787 (1996). No later device cites it as a predicate yet.

K960787 · Tur,Arthroscopic,Cystoscopy Irrigation Sets · Baxter Healthcare Corp · 1996 · recalled1995200020052010201520202025
  1. Root · 1 generation backK960787 Tur,Arthroscopic,Cystoscopy Irrigation SetsBaxter Healthcare Corp · 1996 · Recalled
  2. This deviceK254111 Irrigation/Urology SetsB.Braun Medical, Inc. · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K960787Tur,Arthroscopic,Cystoscopy Irrigation SetsBaxter Healthcare Corp19964
0 (this device)K254111Irrigation/Urology SetsB.Braun Medical, Inc.2026—
FIG. 1 — Lineage of K254111, 1996–2026Source: FDA 510(k) summaries, read by 510(k) Report · 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 summary (predicates and 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.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K960787Tur,Arthroscopic,Cystoscopy Irrigation Sets
Summary page 5
…& Urology Legally marketed device to which equivalence is claimed (predicate) Device Name / 510(k) TUR, Arthroscopic, Cystoscopy Irrigation Sets / K960787 Device Description The proposed B. Braun Irrigation/Urology Sets are sterile, single-use devices intended for the delivery of…
Baxter Healthcare Corp19964

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.

What does this lineage say?

  • Its one ancestor has a 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. 2026, this device’s year, is highlighted.

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?

B. Braun Medical Irrigation Tubing Set is intended for delivery of irrigation solutions from a

container to an irrigation site during bladder irrigation or endoscopic procedures such as cystoscopy and transurethral

resection procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K254111: Irrigation/Urology Sets.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K254111

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Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026