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: ODD FDA class 2

Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula

Gastroenterology, Urology

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The Endoscopic Retrograde Cholangiopancreatography (ERCP) Cannula (product code ODD) is a gastroenterology and urology device used during ERCP procedures to cannulate the bile duct or pancreatic duct for the identification of stones, tumors, or narrowings (strictures) in the biliary tree. The cannula is passed through the endoscope's working channel and into the ampulla of Vater. This device is FDA Class 2 under regulation 876.1500 in the Gastroenterology, Urology specialty, requiring 510(k) clearance and compliance with general and special controls. It carries no implant or life-sustaining flags.

510(k) Clearances

18 matches
K Number
Device Name
Single Use Cannula V PR-V223Q/V414Q/V416Q/V418Q/V420Q/V427Q/V434Q/V435Q; Single Use 2-Lumen Cannula V PR-V614M
BioShield biopsy valve EUS - Linear
Classic ERCP Catheter and Huibregtse-Katon ERCP Catheter and Huibregtse-Katon Angled, Glo-Tip ERCP Catheter, Glo-Tip II Double Lumen ERCP Catheter & w/ Radiopaque Bands, Fusion ERCP Catheter with DomeTip and Fusion OMNI ERCP Catheter with DomeTip, Haber RAMP Catheter, Soehendra Universal Catheter
BIOSHIELD-ERCP BIOPSY VALVE, MODEL 00711138
DISPOSABLE BENDING CANNULA PR-233Q
ALIEN RX MICRO CANNULA, MODEL 4530
WILSON-COOK STRICTURE MEASURING CATHETER
ERCP CANNULA
ENDOSCOPIC CATHETER
BARD BILISYSTEM ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY (ERCP) CANNULA
OLYMPUS PR-23Q DISPOSABLE CANNULA (BALL TIP)
SURGITEK(R) ERCP CONTRAST MEDIA SYSTEM
ENDOSCOPES & ACCESS.(SCLEROTHERAPY/TRANSBRONCHIAL)
DAVOL ERCP CANNULA
ERCP CANNULA
ENDOSCOPIC RETROGRADE
E.R.C.P. CANNULAS
E.R.C.P. CANNULA PRODUCT

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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