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: NYS FDA class 2

Wound Dressing With Poly(Diallyl Dimethyl Ammonium Chloride)(Pdadmac)

General, Plastic Surgery

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The Wound Dressing with Poly(Diallyl Dimethyl Ammonium Chloride) (PDADMAC) (product code NYS) is a sterile barrier wound dressing containing a permanently bound PDADMAC additive on a textile substrate, intended as a primary dressing for exuding wounds, first and second degree burns, and surgical wounds, as well as for securing primary dressings and wound packing. It acts as a physical barrier to external contaminants without releasing antimicrobial agents. Classified as FDA Class 2, it requires 510(k) clearance and is regulated under 21 CFR 878.4015 within the General and Plastic Surgery specialty.

510(k) Clearances

1 matches
K Number
Device Name
QMT NIMBUS ANTIMICROBIAL BARRIER GAUZE DRESSING

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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