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.

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.

Free to try · every answer cites its records

Product Code: KAL FDA class 1

Retractor, Ent

Ear, Nose, Throat

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An ENT retractor is a surgical instrument used to hold back tissue and maintain exposure during ear, nose, and throat surgical procedures, allowing the surgeon access to the operative field. The device is classified as FDA Class 1, indicating low risk, and is subject only to general controls including labeling and manufacturing requirements. Product code KAL is regulated under 21 CFR 874.4420 in the Ear, Nose, Throat medical specialty. No special flags apply to this device.

510(k) Clearances

5 matches
K Number
Device Name
SMALL MASTOID RETRACTOR
ADJUSTABLE FORK RETRACTOR
ALLPORT MASTOID RETRACTORS
RING HANDLE & RETRACTORS
CONVERSE ALTAR RETRACTOR

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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