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: GBZ FDA class 1

Catheter, Cholangiography

General, Plastic Surgery

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The Catheter, Cholangiography (product code GBZ) is a catheter used during surgery to inject contrast media into the bile ducts, enabling radiographic visualization of biliary anatomy and identification of stones or obstructions during cholangiographic examination. It is classified as FDA Class 1, posing minimal risk, subject to general controls only and not requiring premarket notification. The device is regulated under 21 CFR 878.4200 in the General, Plastic Surgery specialty (SU). No special flags apply to this device.

510(k) Clearances

24 matches
K Number
Device Name
PRE-VIEW CHOLANGIOGRAPHY CLAMP
FLEXIBLE LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER
ENDOPATH
MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER
TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE
ANGIOLAPCATH CHOLANGIOGRAPHY KIT
STRYKER ENDOSCOPY CHOLANGIOGRAM KIT
CLARUS CHOLANGIOGRAM CATHETER KIT
OPERATIVE CHOLANGIOGRAM CATHETER
CHOLANGIOGRAPHY CLAMP
CHOLANGIOGRAPHY CATHETER
CHOLANGIOLAPCATH(TM)
LAPAROSCOPIC SUCTION/IRRIGATION PROBE
CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP
SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH
WURTZ CHOLEY CLIP (TM)
MENTOR DUCTAL CATHETERS
LMI CHOLANGIOGRAM TRAY
PTC-6 AND PTC-8 PERCUTANEOUS CHOLANGIOGRAPHY
BILE ENDOPROSTHESIS SET
SUCTION CATHETER TRAYS
ATRIUM THORACIC CATHETER
TRACHESTOMY & NASAL SUCTIONING KIT #-
CATHETER, CHOLANGIOGRAM, OPERATIVE

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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