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: MJN FDA class 2

Catheter, Intravascular Occluding, Temporary

Cardiovascular

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The Temporary Intravascular Occluding Balloon Catheter is a catheter with an inflatable balloon at its tip used to temporarily occlude blood flow in a blood vessel during surgical or endovascular procedures, controlling hemorrhage or isolating vascular territories for treatment. Classified as a Class 2 device under 21 CFR 870.4450 within the Cardiovascular specialty, it requires 510(k) premarket notification. It carries no implant or life-sustaining flags.

510(k) Clearances

50+ matches
K Number
Device Name
Bridge Plus Occlusion Balloon (590-002)
preCARDIA Occlusion System
LANDMARK REBOA Catheter
Fogarty Occlusion Catheter
RenovoCath
AortaSTAT Occlusion Device
Neurescue device
COBRA-OS Kit
Bridge Occlusion Balloon
pREBOA-PRO Catheter
Gatekeeper Balloon Catheter
ER-REBOA PLUS Catheter
RenovoCath
Eclipse 2L
Occlusion Balloon Catheter
Pruitt F3 Carotid Shunt, 10 Fr, Pruitt F3 Carotid Shunt, 9 Fr, Pruitt F3 Carotid Shunt, 8 Fr
Sniper Infusion Catheter with Balloon Occlusion
GORE Molding and Occlusion Balloon Catheter
ER-REBOA Catheter
ER-REBOA Catheter
RenovoCath
REBOA Balloon Catheter
Bridge Occlusion Balloon
Pruitt F3-S Polyurethane Carotid Shunt
Fogarty Occlusion Catheter
Pruitt F3-S Carotid Shunt
PaxWire Occlusion Balloon System
Occlusion Balloon Catheter
RENOVOCATH RC120
EQUALIZER OCCLUSION BALLOON CATHETER
LEMAITRE 8F OCCLUSION CATHETER
OCCLUSION BALLOON CATHETER
PTS-X SIZING BALLOON CATHETER
TRANSFORM OCCLUSION BALLOON CATHETER (COMPLIANT AND SUPER COMPLIANT
SCEPTER C OCCLUSION BALLOON CATHETER
SCEPTER XC OCCLUSION BALLOON CATHETER
TAPAS CATHETER
SCEPTER C OCCLUSION BALLOON CATHETER
PTS-X SIZING BALLOON CATHETER
MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7 MM; MICRUS ASCENT OCCLUSION BALLOON CATHETER 6X9 MM; MICRUS SUMMIT OCCLUSIO
PRUITT CAROTID KIT
DUFLO CATHETER (HEPARIN COATED)
HYPERGLIDE AND HYPERFORM OCCLUSION BALLOON SYSTEMS
HYPERFORM OCCLUSION BALLOON CATHETER, HYPERGLIDE OCCLUSION BALLOON CATHETER, HYPERGLIDE OCCLUSION BALLOON CATHETER MODEL
FOGARTY OCCLUSION CATHETER
HYPERGLIDE OCCLUSION BALLOON SYSTEM, HYPERFORM OCCLUSION BALLOON SYSTEM, MODEL 104-4112, 104-4113, 104-4127,104-4132,104
HYPERGLIDE OCCLUSION BALLOON SYSTEM, MODEL 104-4310, 104-4315
MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7MM,6X9MM, MICRUS SUMMIT OCCLUSION BALLOON CATHETER 4X10MM,4X15, MODEL BRS 00
FLOCONTROL , MODEL 1028
HYPERGLIDE OCCLUSION BALLOON 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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