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: CZP FDA class 2

Iga, Antigen, Antiserum, Control

Immunology

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The IgA, Antigen, Antiserum, Control test system (product code CZP) is an in-vitro diagnostic device used in immunology to measure immunoglobulin A (IgA) concentrations in serum using antigen-antiserum immunochemical methods, with associated control materials for assay verification, supporting the evaluation of immune deficiency and humoral immunity. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification. It falls under regulation 21 CFR 866.5510 in the Immunology medical specialty. This device is eligible for third-party review under the FDA's accredited persons program.

510(k) Clearances

50+ matches
K Number
Device Name
Yumizen C1200 Immunoglobulin A, Yumizen C1200 Immunoglobulin G, Yumizen C1200 Immunoglobulin M
IMMAGE SYSTEMS LOW CONCENTRATION IMMUNOGLOBULIN A REAGENT
ROCHE DIAGNOSTICS TINA-QUANT IGA GEN.2
N LATEX IGA
WAKO IGA II-HA, IMMUNOGLOBULIN CALIBRATOR SET, IMMUNOGLOBULIN STANDRAD
IGA
QUANTEX IGA
IGA IMMUNOTURBIDIMETRIC & CALIBRATOR
BOEHRINGER MANNHEIM IGA ASSAY
N LATEX IGA
IGA SUBCLASS RID KIT FOR DIAGNOSTIC USE
IL TEST IMMUNOGLOBULIN A
TITAN GEL IMMUNOFIX KIT, CAT. NO. 3046
RAICHEM(TM) SPIA(TM) IGA REAGENTS
SPQ(TM) ANTIBODY REAGENT SET II FOR IGA
IMMUNOCHEMICAL DETERMINATION OF IMMUNOGLOBULIN A
TECHNICON DPA-1 IMMUNOGLOBULIN A
WAKO(TM) IGA-HA DIRECT
IMMUNOGLOBULINS A
QM300 IGA, ANTIGEN, ANTISERUM, CONTROL
PRECIMAT (R) IGA, G, M
TINA-QUANT(R) IGA
TDX IMMUNOGLOBULIN A DIAGNOSTIC KIT
DAKO ITA, IMMUNOGLOBULIN A (IGA)
IMMUNOGLOBULINS A,G,M,D,E IMMUNOLOGICAL TEST
QUANTIMETRIC PLUS IGA REAGENT KIT
GILFORD IMMUNOGLOBULIN A REAGENT
RADIAL IMMUNO-DIFFUSION PLATES IGA, IGD, IGG & IGM
SPQ TEST SYSTEM FOR IMMUNOGLOBULIN A
CORNING IMMUNOFIXATION SYS
TISSUE-TEK IMMUNOHISTOLOGY KIT IGA/IGG
AMER. HISTO-ID SYS PRIMARY IGA 2720-21
FITC GOAT ANTI-HUMAN IGA A CHAIN
TIA-IGA REAGENT & CALIBRATOR SETS
IMMUNOGLOBULIN CONTROL
IMMUNOGLOBULIN ASSAYS-IGG, IGA, IGM
IMMUNO DIAGNOSTICS ASSAY
ACA IMMUNOGLOBULIN A/M CALIBRATORS
ACA IMMUNOGLOBIN A TEST PACK
IMMUNOGL. FRCT. OF RABBIT ANTISER.-IGA
GELMAN IG-FIX KIT
AIM SYSTEM (FOR IGA)
AUTOMATED IMMUNOPRECIPITIN METHOD/IGA
J.T. BAKER IMMUNO. A NEPHELOMETRIC ASSAY
GEMENI IGA ASSAY
IMMUNOGLOBULIN A REAGENT SYSTEM
LANCER L-INA ANTI-IGA
ANTISERUM, HUMAN, IGA
A-GENT IMMUNOGLOBULINE TEST SYSTEM
RADIAL IMMUNODIFFUSION KIT-IMMUNOGLOB.

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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