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: DQY FDA class 2

Catheter, Percutaneous

Cardiovascular

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The Percutaneous Catheter is a cardiovascular device designed to be inserted through the skin into a blood vessel using a needle-based percutaneous technique, enabling minimally invasive vascular access for diagnostic or therapeutic interventions. It is classified as an FDA Class 2 device, indicating moderate risk, and requires 510(k) premarket notification before marketing. The product code is DQY and it is regulated under 21 CFR 870.1250 within the Cardiovascular medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Primum Hydrophilic Guiding Catheter
CPS Locator 3D Plus Delivery Catheter
SAT CenterFlow Molding Balloon Catheter (IN20-00313)
FlexiGo 3D Delivery Catheter
Dorado™ PTA Balloon Dilatation Catheter
GORE® Tri-Lobe Balloon Catheter
Shockwave CS Guide Catheter
APRO 45 Catheter
APRO 55 Intermediate Catheter
Amulet™ Steerable Delivery Sheath
FlowGuide (FG60F); GuidionShort (GS60F)
LiquID .051 LP Guide Catheter Extension
SelectSite C304 Deflectable Catheter System (C304); C315 Delivery System (C315)
Seclusion Catheter
Ventrax™ Delivery System
COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL)
MitraClip™ G5 Steerable Guide Catheter (SGC0801); TriClip™ G5 Steerable Guide Catheter (TSGC0801)
SENDERO MAX Delivery Catheter
Shadow Catheter
SSPC NXT Delivery Catheter
CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55)
Selectra 3D Lead Delivery System (443624-443629, 451789-451791); Selectra Slitter Tool (383119); Selectra Accessory Kit (375518)
ShapeIT (SI014135)
TriClip Steerable Guide Catheter
Cordis BRITECROSS Support Catheter
ASAHI Veloute; ASAHI Veloute C3; ASAHI Tellus; ASAHI Tellus C3
React 71 Catheter
APRO 55 Catheter
SENDERO Microcatheter
SINC Support Catheter
WATCHMAN TruSteer Access System (M635TU90050)
Teleport XT Microcatheter
TriSalus TriGuideTM Guiding Catheter
SENDERO Microcatheter
091 Balloon Guide Catheter
Paragon 8F Balloon Guide Catheter
Amulet™ Steerable Delivery Sheath
Microcatheter
Ventrax™ Delivery System (VTR851)
6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter
Rubicon™ Control Support Catheter (H749394323506A1)
R2P Navicross
Micro Rx
5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter
CPS Direct™ Universal slittable outer guide catheter (DS2C029)
Stingray LP Catheter
RayFlow
CPS Locator 3D Delivery Catheter
6F Wallaby Long Sheath
ISAAC Neurovascular Navigation 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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