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: BYS FDA class 2

Oxygenator, Long Term Support Greater Than 6 Hours

Cardiovascular

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The Oxygenator, Long Term Support Greater Than 6 Hours is a device used during prolonged extracorporeal circulation to transfer oxygen into and remove carbon dioxide from the patient's blood outside the body for periods exceeding six hours, as in extended cardiopulmonary bypass or extracorporeal membrane oxygenation (ECMO). It is classified as FDA Class 2, requiring 510(k) premarket notification. The product code is BYS, regulated under 21 CFR 870.4100 in the Cardiovascular specialty. This device is designated as life-sustaining or life-supporting.

510(k) Clearances

3 matches
K Number
Device Name
Nautilus VF ECMO Oxygenator
Nautilus Smart ECMO Module
TUBING PACK, EXTRACORPOREAL, H-3000

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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