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: DRA FDA class 2

Catheter, Steerable

Cardiovascular

View full classification →

The Steerable Catheter is a cardiovascular device with a deflectable tip that can be actively directed by the operator to navigate complex vascular anatomy during diagnostic or interventional procedures. It is classified as an FDA Class 2 device, indicating moderate risk, and requires 510(k) premarket notification before marketing. The product code is DRA and it is regulated under 21 CFR 870.1280 within the Cardiovascular medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

41 matches
K Number
Device Name
Globe Introducer (601-01001)
FARADRIVE™ Steerable Sheath
FlexCath Contour™ Steerable Sheath
POLARSHEATH™ Steerable Sheath 12F (UPN:M004CRBS3150), POLARMAP™ Circular Mapping Catheter (UPN:M004CRBS7210), POLARMAP™ EP Electrical Cable (UPN:M004CRBS62000), SMARTFREEZE™ Esophageal Temperature Sensor (ETS) Cable: -SMARTFREEZE™ Esophageal Temperature Sensor (ETS) Cable (UPN: M004CRBS6310), -SMARTFREEZE™ 16 PIN Esophageal Temperature Sensor (ETS) Cable (UPN: M004CRBS6320), -SMARTFREEZE™ CIRCA Esophageal Temperature Sensor (ETS) Cable (UPN: M004CRBS6340), SMARTFREEZE™ Pressure Sensor
MitraClip G4 Steerable Guide Catheter
AcQGuide® VUE Steerable Sheath
AcQGuide MAX Steerable Sheath
FlexCath Advance Steerable Sheath and Dilator
Steerable Introducer 12F
MitraClip G4 Steerable Guide Catheter
FlexCath Advance Steerable Sheath and Dilator
Steerable Guide Catheter
AcQGuide Steerable Sheath
Hansen Medical Magellan Robotic Catheter 9Fr
Steerable Guide Catheter
HeartLight Deflectable Sheath
Hansen Medical Magellan Robotic Catheter eKit
Hansen Medical Magellan Robotic Catheter 6Fr and Accessory Components
MAGELLAN ROBOTIC CATHETER 6FR (GUIDE AND LEADER), MAGELLAN ROBOTIC CATHETER 6FR ACCESSORY KIT
FLEXCATH ADVANCE STEERABLE SHEATH (12 FRENCH)
ARTISAN EXTEND CONTROL CATHETER
CARIOSOLUTIONS PERCU-PRO STEERABLE INTRODCER 65CM CARIOSOLUTIONS PERCU-PRO STEERABLE INTRODUCER 80CM
Z FLEX-270TM STEERABLE SHEATH
STEERABLE GUIDE CATHETER
FLEXCATH STEERABLE SHEATH (12 FRENCH), FLEXCATH STEERABLE SHEATH (10 FRENCH) MODEL 3FC12, 3FC10
MODIFICATON TO: STEERABLE GUIDE CATHETER, MODEL SGC01ST
EVALVE STEERABLE GUIDE CATHETER
EVALVE STEERABLE GUIDE CATHETER, MODEL SGC01ST
STEERABLE GUIDE CATHETER
FLEXCATH STEERABLE SHEATH & DILATOR, MODELS 3FC10, 3FC12
FLEXCATH STEERABLE SHEATH & DILATOR
LUMINARY CANNULATOR BIDEFLECTABLE CATHETER WITH LUMEN
LYSUS INFUSION SYSTEM
REFLEXION CANNULATOR STEERABLE ELECTROPHYSIOLOGY CATHETER WITH LUMEN, MODEL 402805
24 FR. LEFT HEART VENT CATHETER WITH PRESSURE MONITORING LINE, MODEL 12524
CRI CYNOSAR CATHETER
RESPONSE(TM) STEERABLE CATHETER
CRI CYNOSAR CATHETER
CRI CYNOSAR CATHETER
MICRO-GUIDE SYSTEM
ADULT VENT 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.

Popular Product Codes

Commonly searched