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: NHV FDA class 2

System, Water Purification, General Medical Use

Gastroenterology, Urology

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The Water Purification System for General Medical Use is a portable water treatment device featuring components and technology similar to hemodialysis water treatment systems, but intended for general-purpose water purification in medical settings rather than hemodialysis. Its intended uses include washing surgeons' hands, cleaning surgical instruments, and wound cleansing. It is classified as FDA Class 2 (Special Controls), requiring 510(k) clearance, under product code NHV and regulation 21 CFR 876.5665 in the Gastroenterology and Urology specialty. The device is not an implant and is not life-sustaining.

510(k) Clearances

11 matches
K Number
Device Name
i3 ONE (203100-S);i3 TWO connect (203200-S);i3 TWO direct (203300-S)
FILTRAY 2G Disposable Water Filters
Ecolab POU Water Filter Spray Outlet, Ecolab POU Water Filter Nozzle Outlet, Ecolab POU Water Filter Shower Wand
Ecolab POU Water Filter
Pall QPoint Water Filter Capsule (Shower), Pall QPoint Water Filter Capsule (Faucet)
HydraGuard 10 UltraFilter
NOSOGARD FILTERS
Pall-Aquasafe Water Filter
Nephros S100
NEPHROS DSU-H, NEPHROS SSU-H
MAINSTREAM WATER PURIFICATION DEVICE

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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