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: DXE FDA class 2

Catheter, Embolectomy

Cardiovascular

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The Embolectomy Catheter is a cardiovascular interventional device used to retrieve blood clots from occluded arteries or veins by advancing a balloon catheter past the clot, inflating the balloon, and withdrawing it to extract the embolus and restore vascular patency. It is classified as an FDA Class 2 device, indicating moderate risk, and requires 510(k) premarket notification before marketing. The product code is DXE and it is regulated under 21 CFR 870.5150 within the Cardiovascular medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Fogarty Thru-Lumen Embolectomy Catheter
Fogarty Fortis Arterial Embolectomy Catheter
Fogarty Venous Thrombectomy Catheters
Fogarty Arterial Embolectomy Catheter with Gate Valve
Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters
Merlin Aspiration System
Python Catheter/Over-the-Wire Latis Graft Cleaning Catheter
Fogarty Arterial Embolectomy Catheter, Fogarty Biliary Balloon Probe
Bunegin-Albin Air Aspiration Set
Needle's Eye Snare Retrieval Set - 54cm
Export Advance Aspiration Catheter
EMBO PLUS EMBOLECTOMY CATHETER
PTA-PLUS PTA BALLOON CATHER 5 MM X 4CM, PTA-PLUS PTA BALLOON CATHETER 6MM X 4CM
MEDTRONIC EXPORT AP CATHETER
OVER THE WIRE EMBOLECTOMY CATHETER, MODEL 2302
MODIFICATION TO ATRIUM MEDICAL CORPORATION CLEARWAY PTFE BALLOON CATHETER
MULTI-SNARE SET
ATRIUM MEDICAL CORPORATION CLEARWAY PTFE BALLOON CATHETER
LEMAITRE IRRIGATION CATHETER
LEMAITRE VENOUS THROMBECTOMY CATHETER
LEMAITRE BALLOON CATHETER WITH IRRIGATION
LEMAITRE EMBOLECTOMY CATHETER
BIOSENSORS EMBOLECTOMY CATHETER
ARROW 5FX60CM BALLOON EMBOLECTOMY CATHETER, MODEL # EM-56025
DCAT EMBOLECTOMY CATHETER SYSTEM
AMPLATZ GOOSE NECK SNARE KIT/ CATHETER
LATIS GRAFT CLEANING CATHETER
EMBOLECTOMY, IRRIGATION - OCCLUSION BALLOON CATHETER BY J-LLOYD MEDICAL, INC.
SINGLE LUMEN EMBOLECTOMY CATHETER
LMI IRRIGATION CATHETER (IGR)
LMI THROMBECTOMY CATHETER
DUAL LUMEN EMBOLECTOMY CATHETER
VERSA-CATH ARTERIAL CATHETER
NEEDLE'S EYE SNARE
VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE
LMI ARTERIAL EMBOLECTOMY CATHETER
LMI OCCLUSION CATHETER
AVD INTIMAX THROMBECTOMY CATHETER
ARTERIAL EMBOLECTOMY
WELTER SNARE RETRIEVER
J-LLOYD ARTERIAL EMBOLECTOMY CATHETER
DUAL BALLOON EMBOLECTOMY CATHETER
INTIMAX THROMBECTOMY CATHETER
CATHLAB SILICONE ARTERIAL EMBOLECTOMY CATHETER
EMBOLECTOMY CATHETER
AMPLATZ GOOSE-NECK SNARE
ARTERIAL EMBOLECTOMY CATHETER
ARTERIAL EMBOLECTOMY CATHETER
FOGARTY ARTERIAL EMBOLECTOMY II CATHETER
3F AND 4F IRRIGATION EMBOLECTOMY 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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