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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: QNR FDA class 2

Blood Pump For Ecmo, Long-Term (> 6 Hours) Use

Cardiovascular

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The Blood Pump for ECMO Long-Term (greater than 6 hours) Use is a cardiovascular device intended as part of an extracorporeal membrane oxygenation (ECMO) circuit to provide assisted extracorporeal circulation and physiologic gas exchange for patients with acute respiratory failure or acute cardiopulmonary failure where other treatments have failed and continued deterioration is expected or death is imminent. This device is classified as FDA Class 2, requiring 510(k) clearance, under regulation 870.4100 in the Cardiovascular specialty. It carries product code QNR, is life-sustaining, and is not an implant.

510(k) Clearances

8 matches
K Number
Device Name
VitalFlow Console
CentriMag™ Acute Circulatory Support System
LifeSPARC System
VitalFlowTM Centrifugal Pump
VitalFlow™ Console
CentriMag™ Blood Pump for use with CentriMag™ Acute Circulatory Support System
LifeSPARC System
TandemHeart Pump and Escort Controller

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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