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: QJP FDA class 2

Catheter, Percutaneous, Neurovasculature

Cardiovascular

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The Catheter, Percutaneous, Neurovasculature is a Class 2 cardiovascular device intended to provide vascular access to the neurovasculature for interventional or diagnostic procedures, such as cerebral angiography or neurointerventional therapy. It requires 510(k) clearance and is regulated under 21 CFR 870.1250, reviewed by the Neurology panel under the Cardiovascular medical specialty. The product code is QJP. The device is not an implant and is not flagged as life-sustaining.

510(k) Clearances

50+ matches
K Number
Device Name
FUBUKI XF-R Neurovascular Long Sheath
Branchor X Balloon Guide Catheter
93 NeuFlex Catheter
PATH BGC
Excelsior XT-27 Microcatheter, Excelsior XT-27 Flex Microcatheter, Excelsior XT-27 Pre-Shaped Microcatheter, Excelsior XT-27 Flex Pre-Shaped Microcatheter
AXS Lift Intracranial Base Catheter
VersaD Delivery Catheter
Radical the Dude 8F Guide Catheter
APRO 70 Swift Catheter
Rist 079 Radial Access Guide Catheter; Rist 071 Radial Access Guide Catheter; Rist Radial Access Selective Catheter
Next Generation Access Platform
Broadway 8 Catheter
Echo Intracranial Base Catheter
Access25™ Delivery Microcatheter
87 NeuGlide Catheter
Socrates 38 Catheter
Neurovascular Access System Family
Zipline Access Catheter
CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter
8F Modified Sheath System
Next Generation Access Catheter
TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform; Zoom 88 Large Distal Platform Support
Wedge XL Delivery Catheter
CEREGLIDE 92 Catheter System
EMBOGUARD Balloon Guide Catheter
MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter)
Esperance Distal Access Catheter
Distal Access Catheter
Distal Access Catheter
Millipede 088 Access Catheter
Slinky Catheter
Radical the Dude 7F Guide Catheter
CEREGLIDE 92 Intermediate Catheter
Millipede 088 Access Catheter
Q Distal Access Catheter
SOFIA EX Intracranial Support Catheter
NG Delivery Catheter
Plato 17 Microcatheter
Route 92 Medical Full Length 054 Access System
SelectFlex Neurovascular Access System Family
TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform; Zoom 88 Large Distal Platform Support
CEREGLIDE 71 Intermediate Catheter
CELLO II Balloon Guide Catheter
BENCHMARK BMX81 Access System
Branchor Balloon Guide Catheter
Route 92 Medical Full Length 070 Access System
Millipede 088 Access Catheter
Benchmark BMX96 Access System
Minjie Catheter System
Distal Access Catheter

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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