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: NHX FDA class 2

Antibodies, Anti-Cyclic Citrullinated Peptide (Ccp)

Immunology

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The Anti-Cyclic Citrullinated Peptide (CCP) Antibodies test is an in vitro diagnostic device used for the detection of anti-CCP antibodies in human serum or plasma, serving as an aid in the diagnosis of rheumatoid arthritis. It is classified as FDA Class 2 (Special Controls), requiring 510(k) clearance, under product code NHX and regulation 21 CFR 866.5775 in the Immunology specialty. The device is eligible for third-party review and is not an implant or life-sustaining device.

510(k) Clearances

21 matches
K Number
Device Name
ADVIA Centaur Anti-CCP IgG (aCCP) assay including Reagents and Calibrators, Quality Controls and Master Curve Materials.
QUANTA Flash CCP3, QUANTA Flash CCP3 Calibrators, and QUANTA Flash CCP3
IMMULITE 2000 ANTI-CCP IGG ASSAY
MULTI-ANALYTE DETECTION SYSTEMS
AXIS-SHIELD ANTI-CCP
CCPOINT
BIOPLEX 2200 ANTI-CCP KIT ON THE BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM
THERATEST EL-ANTI-CCP/2
IMMUNOSCAN CCPLUS
ARCHITECT ANTI-CCP (100 TEST), ARCHITECT ANTI-CCP (500 TEST), MODELS 1P65-25, 1P65-35
ROCHE ELECSYS ANTI-CCP IMMUNOASSAY, ROCHE ELECSYS PRECICONTROL ANTI-CCP
QUANTA LITE CCP3.1 IGG/IGA ELISA
EUROIMMUN ANTI-CCP ELISA
AXSYM ANTI-CCP REAGENT, STANDARD CALIBRATOR AND CONTROL KITS, MODELS 3L91-20, 3L91-01 AND 3L91-10
EDIA ANTI-CCP
ELIA CCP, MODEL 14-5515-01; ELIA CCP CONTROL, MODEL 83-1009-01
IMMUNOSCAN RA ANTI-CCP TEST SYSTEM
QUANTA LITE CCP3 IGG ELISA
DIASTAT ANTI CYCLIC CITRULLINATED PEPTIDE (ANTI-CCP) ELISA
DIASTAT ANTI CYCLIC CITRULLINATED PEPTIDE ELISA, MODEL FCCP 200
QUANTA LITE CCP ELISA

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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