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: NRJ FDA class 2

Ultrasound, Skin Permeation

General, Plastic Surgery

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The Skin Permeation Ultrasound device uses low-frequency ultrasound energy to temporarily disrupt the outer layer of the skin, enabling the transdermal application of drugs or other substances. This technology, known as sonophoresis, facilitates drug delivery through skin without needles. It is an FDA Class 2 device regulated under 21 CFR 878.4410 in the General and Plastic Surgery specialty, with product code NRJ, requiring 510(k) clearance. Third-party 510(k) review is available for this device. It is not an implant and does not provide life-sustaining support.

510(k) Clearances

1 matches
K Number
Device Name
SONOPREP ULTRASONIC SKIN PERMEATION SYSTEM AND TOPICAL ANESTHETIC KIT, MODEL D2000

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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