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: LOX FDA class 2

Catheters, Transluminal Coronary Angioplasty, Percutaneous

Cardiovascular

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Percutaneous transluminal coronary angioplasty (PTCA) catheters are used to dilate narrowed or blocked coronary arteries by advancing a balloon-tipped catheter to the site of obstruction and inflating the balloon under hydraulic pressure. According to its definition, a PTCA catheter operates on the principle of hydraulic pressurization applied through an inflatable balloon attached to the distal end of the catheter. It is classified as a Class 2 (moderate risk) device, subject to general controls and special controls, and requires 510(k) premarket notification before marketing. The product code is LOX, regulated under 21 CFR 870.5100, within the Cardiovascular medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
Pantera Pro; Pantera LEO
Sapphire NC ULTRA Coronary Dilatation Catheter
Sapphire ULTRA Coronary Dilatation Catheter
Ringer perfusion balloon catheter, 2.00 x 20mm (5881); Ringer perfusion balloon catheter, 2.50 x 20mm (5882); Ringer perfusion balloon catheter, 2.50 x 30mm (5883); Ringer perfusion balloon catheter, 3.00 x 20mm (5884); Ringer perfusion balloon catheter, 3.00 x 30mm (5885); Ringer perfusion balloon catheter, 3.50 x 20mm (5886); Ringer perfusion balloon catheter, 3.50 x 30mm (5887); Ringer perfusion balloon catheter, 4.00 x 20mm (5888); Ringer perfusion balloon catheter, 4.00 x 30mm (58
Firefighter™ NC Pro PTCA Balloon Catheter
Coronary Dilatation Balloon Catheter (VesPenetrator®), Coronary Dilatation Balloon Catheter (VesTraveler®), Coronary Dilatation Balloon Catheter (VexPander®)
POT PTCA Balloon Dilatation Catheter
SC HONKYTONK PTCA Balloon Dilatation Catheter
NC ROCKSTAR Non-Compliant PTCA Balloon Dilatation Catheter
NC TREK NEO Coronary Dilatation Catheter
Emerge Monorail PTCA Dilatation Catheter
OPN NC PTCA Dilatation Catheter
Selebrek PTCA Balloon Dilatation Catheter
Sapphire NC 24
Tamarin Blue PTCA RX Dilatation Catheter
Selethru(TM) NC PTCA Balloon Dilatation Catheter
KardiFlex NC Coronary Dilatation Catheter
KardiFlex PTCA Balloon Dilatation Catheter
Artimes pro Balloon Dilatation Catheter
Sapphire II PRO
Sapphire NC Plus Coronary Dilatation Catheter
Selethru PTCA Balloon Dilatation Catheter
NC TREK™ RX Coronary Dilatation Catheter; NC TREK™ OTW Coronary Dilatation Catheter; TREK™ RX Coronary Dilatation Catheter; TREK™ OTW Coronary Dilatation Catheter; MINI TREK™ RX Coronary Dilatation Catheter; MINI TREK™ OTW Coronary Dilatation Catheter; MINI TREK™ II OTW Coronary Dilatation Catheter
Sapphire II PRO Balloon Dilatation Catheter
Mozec – Rx PTCA Balloon Dilatation Catheter, Mozec NC – Rx PTCA Balloon Dilatation Catheter
OTW Takeru PTCA Balloon Dilatation Catheter
Sapphire II PRO
Gallant PTCA Dilatation Catheter
RX NC Takeru PTCA Balloon Dilatation Catheter
SeQuent Neo Percutaneous Transluminal Coronary Angioplasty (PTCA) Balloon Catheters
RX Takeru Balloon Dilatation Catheter
Pantera LEO
NC Gallant PTCA Catheter
Sapphire II PRO
Emerge PTCA Dilatation Catheter
Maverick XL Percutaneous Transluminal Coronary Angioplasty Monorail Dilatation Cathete
Pantera Pro
Sapphire NC Plus
Apollo Balloon Dilatation Catheter
Mozec NC-Rx PTCA Baloon Dilatation Catheter
NC Quantum Apex PTCA Dilatation Catheter
Chocolate XD PTCA Balloon Catheter
FLASH Mini Ostial System - 3.0mm x 8mm x 135cm, FLASH Mini Ostial System - 3.5mm x 8mm x 135cm, FLASH Mini Ostial System - 4.0mm x 8mm x 135cm, FLASH Mini Ostial System - 4.5mm x 8mm x 135cm
FILAO NC RX PTCA DILATATION CATHETER
Chocolate PTCA Balloon Catheter
Euphora Rapid Exchange Balloon Dilatation Catheter
FOXTROT NC PTCA Balloon Catheter
APOLLO BALLOON DILATATION CATHETER
ARTIMES BALLOON DILATATION CATHETER
NC EUPHORA RAPID EXCHANGE BALLOON DILATATION 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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