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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: PQK FDA class 2

Percutaneous Catheter For Creation Of An Arteriovenous Fistula For Hemodialysis Access

Cardiovascular

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The Percutaneous Catheter for Creation of an Arteriovenous Fistula for Hemodialysis Access is a single-use percutaneous catheter system that creates an arteriovenous fistula in the arm of patients with chronic kidney disease who require hemodialysis, providing long-term vascular access. It is classified as FDA Class 2 under 21 CFR 870.1252 in the Cardiovascular specialty, requiring 510(k) premarket notification. The device enables minimally invasive creation of AV fistulae as an alternative to open surgery. Product code PQK; not an implant and not life-sustaining.

510(k) Clearances

7 matches
K Number
Device Name
WavelinQ Plus EndoAVF System
Ellipsys Vascular Access System (Ellipsys System), Power Controller, Ellipsys Vascular Access System (Ellipsys System), Catheter, Ellipsys Vascular Access System (Ellipsys System), Needle
WavelinQ 4F EndoAVF System
Ellipsys Vascular Access System (Ellipsys System), Power Controller, Ellipsys Vascular Access System (Ellipsys System), Catheter, Ellipsys Vascular Access System (Ellipsys System), Crossing Needle
Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005)
Ellipsys Vascular Access System
everlinQ endoAVF System

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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