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: LRD FDA class 1

Applicator, Ent Drug

Ear, Nose, Throat

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An ENT drug applicator is a device used to apply topical medications to the ear, nose, or throat, such as wicks, pledgets, or delivery instruments designed to place or dispense therapeutic agents within these anatomical regions. It is classified as a Class 1 (lowest risk) device, subject only to general controls, representing the least burdensome regulatory category. The product code is LRD, regulated under 21 CFR 874.5220, within the Ear, Nose, and Throat medical specialty. This device is exempt from Good Manufacturing Practice (GMP) requirements under the Quality System regulation.

510(k) Clearances

6 matches
K Number
Device Name
AROMAPATCH
AMSCO STERILE RECOVERIES SURGICAL PACKS
MISTASSIST
THE EXPANDACELL EAR PACK
SURGICAL TRAY (STERILE)
AEROSOL DELIVERY SYSTEMS

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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