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: OWQ FDA class 2

Reprocessed Intravascular Ultrasound Catheter

Cardiovascular

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The Reprocessed Intravascular Ultrasound Catheter is a reprocessed cardiovascular device used for intracardiac and intraluminal visualization of cardiovascular anatomy and physiology. It is classified as Class 2 (FDA Class 2), requiring 510(k) premarket clearance. The product code is OWQ, with regulation number 870.1200 under the Cardiovascular medical specialty.

510(k) Clearances

30 matches
K Number
Device Name
Medline ReNewal Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter (8F, 8FG, 10F, 10FG)
NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)
Medline ReNewal Reprocessed Siemens ACUSON AcuNav 10F Ultrasound Catheter (for Siemens Systems) (08255790 ); Medline ReNewal Reprocessed Siemens ACUSON AcuNav 10F Ultrasound Catheter (for GE Systems) (10043342)
Medline ReNewal Reprocessed Siemens ACUSON AcuNav 8F Ultrasound Catheter (for Siemens Systems) (10135936); Medline ReNewal Reprocessed Siemens ACUSON AcuNav 8F Ultrasound Catheter (for GE Systems) (10135910)
Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheter
Vein360 Reprocessed Visions PV.014P Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter
Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter
Reprocessed ViewFlex Xtra ICE Catheter (D087031)
ViewFlex™ Eco Reprocessed ICE Catheter
Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter
ViewFlex™ Eco Reprocessed ICE Catheter
NES Reprocessed Eagle Eye Platinum RX Digital IVUS Catheter
ViewFlex Xtra Reprocessed ICE Catheter
Reprocessed Eagle Eye Platinum RX Digital IVUS Catheter
Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter
Reprocessed ViewFlex™ Xtra ICE Catheter
Reprocessed ViewFlex Xtra ICE Catheter
Reprocessed Visions PV .035 Digital IVUS Catheter
Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter
Reprocessed AcuNav Diagnostic Ultrasound Catheter
Reprocessed SoundStar 3D Diagnostic Ultrasound Catheter
SoundStar eco 8F 3D Diagnostic eco Ultrasound Catheters, SoundStar eco 8F G 3D Diagnostic eco Ultrasound Catheters
Reprocessed Diagnostic Ultrasound Catheter
REPROCESSED ULTRASOUND INTRACARDIAC ECHO CATHETER
REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETER
REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETERS, MODEL SNDSTR10
REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER
REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER
STERILEMED REPROCESSED IVUS IMAGING CATHETER
REPROCESSED IMAGING 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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