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.

Product Code: NXO FDA class 2

Calprotectin, Fecal

Immunology

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The Calprotectin, Fecal device (product code NXO) is an in vitro diagnostic immunoassay used to measure fecal calprotectin, a neutrophilic protein marker of mucosal inflammation, in human stool samples, aiding in the diagnosis of inflammatory bowel disease (IBD), Crohn's disease, and ulcerative colitis, and helping differentiate IBD from irritable bowel syndrome. It is classified as FDA Class 2, requiring 510(k) clearance, and is regulated under 21 CFR 866.5180 within the Immunology specialty. Third-party 510(k) review is available for this device type.

510(k) Clearances

15 matches
K Number
Device Name
BÜHLMANN fCAL® turbo and CALEX® Cap
ALPCO Calprotectin Immunoturbidimetric Assay
LIAISON Calprotectin, LIAISON Q.S.E.T. Device Plus
ALPCO Calprotectin Chemiluminescence ELISA, ALPCO Easy Stool Extraction Device
Buhlmann fCAL turbo and CALEX Cap
CalprestNG, EasyCal
Calprest, EasyCal
BUHLMANN fCAL turbo
LIAISON Calprotectin, LIAISON Calprotectin Control Set, LIAISON Calprotectin Calibration Verifiers, LIAISON Q.S.E.T. Buffer, LIAISON Q.S.E.T. Device
QUANTA Flash Calprotectin and Fecal Extraction Device
BUHLMANN fCAL ELISA
QUANTA Flash Calprotectin Reagents, QUANTA Flash Calprotectin Calibrators, QUANTA Flash Calprotectin Controls, QUANTA Flash Calprotectin Extraction Buffer
Calprest NG
CALPREST
PHICAL TEST

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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