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: EZL FDA class 2

Catheter, Retention Type, Balloon

Gastroenterology, Urology

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The Balloon Retention-Type Catheter (product code EZL) is an indwelling urinary catheter fitted with an inflatable balloon near its tip that is inflated after insertion to keep the catheter in position within the bladder. It is an FDA Class 2 device (moderate risk), requiring 510(k) premarket notification. It is regulated under 21 CFR 876.5130 in the Gastroenterology and Urology specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Silicone Urethral Catheter (Silicone Urethral Catheter)
InnoCare Specialty Foley Catheter
Rüsch Latex Gold Foley Catheter
TraumaGuard Intra-abdominal Pressure Sensing System
Folysil Silicone Catheter
2-Way 100% Silicone Cleartract Catheter
Teleflex Rusch SoftSimplastic Foley Catheters
Flume Catheter
Accuryn Monitoring System, Accuryn SmartFoley IAP UO Temp Tray System 12 F, Accuryn SmartFoley IAP UO Temp Tray System 14 F
2-Way 100% Silicone Cleartract Catheter
2-Way 100% Silicone ClearTract Catheter
FLUME catheter
Well Lead All Silicone Foley Catheter with Temperature Sensor
Foley Balloon Catheter for Urology
Prefilled Syringe
HDX 100% Silicone 2-way Foley Catheter, 14Fr/10cc, HDX 100% Silicone 2-way Foley Catheter, 16Fr/5cc, HDX 100% Silicone 2-way Foley Catheter, 18Fr/10cc
AquaFlate Pre-Filled Sterile Water Syringe 10mL
Silicone Foley Catheter
Urethrotech UCD
Signal Catheter
PSM 3-Way Silicone Foley Catheter
Bard Vertus Foley Catheter
AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water
Radiance(TM) Clear Sharklet(R) Silicone Foley Catheter
CystoSure Plus Catheter
Yikang Latex Foley Catheter
Silicone Foley Catheter for single use
Duette 100% Silicone Dual-Balloon, Temperature-Sensing Catheter
Kohli Urinary Drainage Catheter
Rusch Silicone Foley Catheter
Rusch Simplastic Foley Catheters
Accuryn Monitoring System
SilverCoat Silicone Foley Catheter
Bard LubriGuard Foley Catheter
Medline Silicone Foley Catheter
WELL LEAD HYDROPHILIC SILICONE FOLEY CATHETER
LIGHTHOUSE URINARY CATHETER
LIGHTHOUSE(TM) URINARY CATHETER
DISPOSABLE SILICONE FOLEY CATHETER
TEMPERATURE SENSOR CATHETER
DIRECTVISION CATHETER, UNCOATED
COUDE/ OR TIEMANN
AMSURE 3-WAY HYDROPHILIC LATEX FOLEY CATHETER
WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR
3 WAY SILICONE FOLEY BALLOON CATHETER
AMSURE HYDROPHILIC LATEX FOLEY CATHETER
PERCUCATH URINARY CATHETER
UC-CARE POSITIONING SYSTEM
WELL LEAD SILICONE AND LATEX FOLEY CATHETERS
BARDEX LUBRI-SIL AND BARDEX LUBRI-SIL I.C. ANTI-INFECTIVE ALL-SILICONE FOLEY CATHETERS

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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