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: NCX FDA class 2

System, Hypothermia, Intravenous, Cooling

Cardiovascular

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The System, Hypothermia, Intravenous, Cooling (product code NCX) is a cardiovascular device that delivers cooled saline or fluid intravenously to induce systemic hypothermia, typically used in cardiac arrest resuscitation or neuroprotection protocols. It is an FDA Class 2 device within the Cardiovascular specialty, requiring 510(k) premarket clearance. No specific regulation number has been assigned to this product code. The device is not flagged as an implant but is associated with critical care applications.

510(k) Clearances

26 matches
K Number
Device Name
Solex 7 Intravascular Heat Exchange Catheter, Cool Line Intravascular Heat Exchange Catheter, ICY Intravascular Heat Exchange Catheter, Quattro Intravascular Heat Exchange Catheter, Thermogard XP Console, Thermogard HQ Console
Solex 7 Intravascular Heat Exchange Catheter, Cool Line Intravascular Heat Exchange Catheter, ICY Intravascular Heat Exchange Catheter, Quattro Intravascular Heat Exchange Catheter, Thermogard HQ Start-Up Kit, Thermogard HQ Start-Up Kit EX, Thermogard HQ Console
Solex 7 Intravascular Heat Exchange Catheter, Cool Line Intravascular Heat Exchange Catheter, ICY Intravascular Heat Exchange Catheter, Quattro Intravascular Heat Exchange Catheter, Start-Up Kit, Coolgard 3000 Console, Thermogard XP Console
TEMPEDY
Hypocore
Solex 7 Intravascular Heat Exchange Catheter, ZOLL Start-Up Kit
Start-Up Kit (SUK), Cool Line Intravascular Heat Exchange Catheter, ICY Intravascular Heat Exchange Catheter, Quattro Intravascular Heat Exchange Catheter
SOLEX INTRAVASCULAR HEAT EXCHANGE CATHETER
COOL LINE CATHETER, MODEL CL-2295A, ICY CATHETER, MODEL IC-3893A AND QUATTRO CATHETER, MODEL IC-4593
INNERCOOL THERAPIES, INC., RAPIDBLUE SYSTEM
SOLEX CATHETER, MODEL SL2593
ARCTIC BLAST INTRAVENOUS FLUID CHILLER
THERMOGARD XP THERMAL REGULATION SYSTEM
REPRIEVE ENDOVASCULAR TEMPERATURE THERAPY SYSTEM
REPRIEVE ENDOVASCULAR TEMPERATURE THERAPY SYSTEM
QUATTRO CATHETER MODEL IC4593
THERMOGARD THERMAL REGULATION SYSTEM
REPRIEVE ENDOVASCULAR TEMPERATURE THERAPY SYSTEM
COOLGARD 3000
ICY CATHETER, MODEL IC-3893A
COOL LINE CATHETER KIT, MODELS CL-2085B, CL-2295A; ICY CATHETER KIT, MODEL IC-3585A; FORTIUS CATHETER KIT, MOD. FR-5093B
CELSIUS CONTROL SYSTEM
ALSIUS COOLGARD 3000 & ALSIUS CATHETER SYSTEM
COOLGARD 3000, COOLINE, START-UP, MODELS 3000, CL-2085B, CL-2295A, CG-500D
CELSIUS CONTROL SYSTEM
SETPOINT ENDOVASCULAR TEMPERATURE MANAGEMENT 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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