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.
Extracorporeal System For Carbon Dioxide Removal
Cardiovascular
The Extracorporeal System for Carbon Dioxide Removal is a cardiovascular device system providing assisted extracorporeal removal of carbon dioxide from a patient's blood in patients with acute respiratory failure where other treatments have failed and continued clinical deterioration is expected or the risk of death is imminent. The system includes a console, software, and disposables such as a gas exchanger, blood pump, cannulae, tubing, filters, and other accessories. This device is classified as FDA Class 2, requiring 510(k) clearance, under regulation 870.4150 in the Cardiovascular specialty. It carries product code QOH and is not an implant and not life-sustaining.
510(k) Clearances
1 matchesWhat 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.