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: OBJ FDA class 2

Catheter, Ultrasound, Intravascular

Cardiovascular

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The Intravascular Ultrasound Catheter (product code OBJ) is a cardiovascular device designed for intracardiac and intraluminal visualization of cardiovascular anatomy and physiology using ultrasound imaging. It enables real-time assessment of vessel wall morphology, plaque characteristics, and lumen dimensions to guide interventional procedures. This device is FDA Class 2 under regulation 870.1200 in the Cardiovascular specialty, subject to 510(k) clearance and general and special controls. It carries no implant or life-sustaining flags.

510(k) Clearances

50+ matches
K Number
Device Name
ViewFlex™ Xtra ICE Catheter; ViewFlex™ Eco Reprocessed ICE Catheter; Advisor™ HD Grid Mapping Catheter, Sensor Enabled™; Advisor™ HD Grid X Mapping Catheter, Sensor Enabled™; Agilis™ NxT Steerable Introducer; Agilis™ NxT Steerable Introducer Dual-Reach™
ViewFlex™ X ICE Catheter, Sensor Enabled™
VeriSight Intracardiac Echocardiography Catheter (VSICE2D); VeriSight Pro Intracardiac Echocardiography Catheter (VSICE3D)
VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System
NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter
SOUNDSTAR™ CRYSTAL Ultrasound Catheter
Provisio™ SLT IVUS™ System
AcuNav Crystal Ultrasound Catheter
OptiCrossTM HD Coronary Imaging Catheter, OptiCrossTM 6 HD Coronary Imaging Catheter
NUVISION™ NAV Ultrasound Catheter
ViewFlex Xtra ICE Catheter
OptiCross™ 18 Peripheral Imaging Catheter
OptiCross, OptiCross HD, OptiCross 6, OptiCross 6 HD
ACUSON AcuNav Volume Intracardiac Echocardiography(ICE) Catheter
NuVision ICE Catheter
ACUSON AcuNav Volume Intracardiac Echocardiography(ICE) Catheter
VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter
NES Reprocessed Visions PV .014P RX Digital IVUS Catheter
Reconnaissance PV .018 OTW Digital IVUS Catheter
ACIST HDi System, ACIST Kodama Intravascular Ultrasound Catheter
ACIST Kodama Intravascular Ultrasound Catheter, ACIST HDi System
Novasight Hybrid System
OptiCross 6 HD, 60 MHz Coronary Imaging Catheter (Paper DFU), OptiCross 6 HD, 60 MHz Coronary Imaging Catheter (e-DFU)
ACUSON AcuNav Volume Intracardiac Echocardiography Catheter
OptiCross HD, 60 MHz Coronary Imaging Catheter (Paper DFU); OptiCross HD, 60 MHz Coronary Imaging Catheter (e-DFU)
ACIST Kodama Intravascular Ultrasound Catheter, ACIST HDi System
AcuNav Diagnostic Ultrasound Catheter 8F,10F
AcuNav V 10F Ultrasound Catheter
AcuNav Volume ICE Catheter
REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip
OptiCross 18, 30 MHz Peripheral Imaging Catheter
OptiCross X, 40 MHz Coronary Imaging Catheter
OptiCross 6, 40 MHz Coronary Imaging Catheter (US Distribution), OptiCross 6, 40 MHz Coronary Imaging Catheter (EU Distribution), OptiCross 6, 40 MHz Coronary Imaging Catheter (Intercontinental Distribution)
Visions PV .035 Digital IVUS Catheter
Visions PV.014P RX Digital IVUS Catheter
Volcano Visions PV .018 Digital IVUS Catheter
EAGLE EYE PLATINUM CATHETER, EAGLE EYE PLATINUM SHORT TIP CATHETER, VISIONS PV .014 PLATINUM
ARROW VPS STYLET PLUS AND CG+ ARROW PICC POWERED BY ARROW VPS STYLET PLUS
VIEWFLEX XTRA ICE CATHETER
SOUNDSTAR ECO 8F GULTRASOUND CATHETER, SOUNDSTAR ECO 8F ULTRASOUND CATHETER
CG+ ARROW JACC POWERED BY ARROW VPS STYLET
OPTICROSS 40 MHZ CORONARY IMAGING CATHETER
VASCULAR POSITIONING SYSTEM (VPS) G4 CONSOLE
HD-IVUS ULTRASOUND IMAGING SYSTEM
VISIONS PV .035 DITITAL IVUS CATHETER
KODAMA INTRAVASCULAR ULRASOUND CATHETER
EAGLE EYE PLATINUM ST CATHETER
SOUNDSTAR ECO DIAGNOSTIC ULTRASOUND CATHETER
ATLANTIS SR PRO2 CORONARY IMAGING CATHETER, ICROSS CORONARY IMAGING CATHETER
VASCULAR POSITIONING SYSTEM TM (VPS TM SYSTEM) STYLET

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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