Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: LJH FDA class 2

System, Irrigation, Urological

Gastroenterology, Urology

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A urological irrigation system is a device used to deliver sterile irrigating solutions into the urological tract during endoscopic or surgical procedures of the bladder, ureter, or urethra, maintaining a clear operative field and preventing tissue desiccation and debris accumulation. The device is FDA Class 2, indicating moderate risk and requiring 510(k) premarket clearance. It carries product code LJH and is regulated under 21 CFR 876.5130 within the Gastroenterology and Urology specialty. This device is eligible for third-party review.

510(k) Clearances

28 matches
K Number
Device Name
Karl Storz UROMAT E.A.S.I.
AMSURE BLADDER IRRIGATION SET
MODIFCATION TO: SPYGLASS IRRIGATION SYSTEM
SPYGLASS IRRIGATION SYSTEM
NEXUS IRRIGATION TUBING SET
URO PRO
PIGGYBACK IRRIGATING SYSTEM
IRRIGATION SETS
MED-RX IRRIGATION SET, MODEL 10-3001, 10-3002, 10-4000, 10-4001
CONTINUOUS FLOW Y-TUBING
FLO ASSISTANT, MODEL 4-250-00
MTP UROPUMP DISPOSABLE TUBING SET
KSEA UROPUMP
ENDO FMS UROLOGY
KARL STORZ MODEL 203020 20 EQUIMAT
MEDLINE Y-TYPE TUR/BLADDER IRRIGATION SET
NHMC IRRIGATION TRAY
TUR,ARTHROSCOPIC,CYSTOSCOPY IRRIGATION SETS
NORTHGATE FLOW ASSIST TUBING FOR UROLOGY
AQUISEN
SURGACTIVATOR
URO-FLO
KSEA DISPOSABLE TUBING SET FOR THE UROMAT PUMP
THE KARL STORZ UROMAT(TM)
PRO PULSE SYRINGE IRRIGATION SYSTEM
FILLING VOLUME OPTION
STERILE FLUID PRODUCING UNIT #EP550
SOLID STATE CONTINUOUS FLOW CONTROL

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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