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: QEB FDA class 2

Ventilatory Electrical Impedance Tomograph

Anesthesiology

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The Ventilatory Electrical Impedance Tomograph is a prescription, non-invasive, non-radiological ventilatory device that provides an assessment of local impedance variation within a cross-section of a patient's thorax, used to monitor regional lung ventilation distribution. It is classified as FDA Class 2, requiring 510(k) premarket notification under regulation 868.1505 in the Anesthesiology specialty. The product code is QEB. It is not an implant and is not life-sustaining.

510(k) Clearances

4 matches
K Number
Device Name
AirTom
Enlight 2100
Enlight 2100
Enlight 1810

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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