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.
Let the assistant find your predicates
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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Device System, Imaging, Tympanic Membrane And Middle Ear
Radiology
The Device System, Imaging, Tympanic Membrane And Middle Ear is a Class 2 imaging device intended for use as a visualization tool for the human tympanic membrane and middle ear space, aiding clinicians in otological examination and assessment. It requires 510(k) clearance and is regulated under 21 CFR 892.1560, reviewed by the Ear, Nose, and Throat panel under the Radiology medical specialty classification. The product code is QJG. The device is not an implant and is not life-sustaining.
510(k) Clearances
2 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.