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: CGN FDA class 2

Acid, Folic, Radioimmunoassay

Clinical Chemistry

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The Radioimmunoassay, Folic Acid test system (product code CGN) is an in-vitro diagnostic device used in clinical chemistry to measure folic acid (folate) levels in serum or whole blood using a radioimmunoassay method, supporting the diagnosis of folate deficiency and related conditions. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification. It falls under regulation 21 CFR 862.1295 in the Clinical Chemistry 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
Elecsys Folate III
Access Folate Assay
LIAISON® Folate
Atellica IM Folate Assay
Diazyme Folate Assay , Diazyme Folate Calibrator Set, Diazyme Folate Control Set
ELECSYS FOLATE III
ROCHE ELECSYS FOLATE RBC; ROCHE ELECSYS FOLATE RBC CALSET
ARCHITECT FOLATE REAGENTS, ARCHITECT FOLATE CALIBRATORS, AND ARCHITECT FOLATE CONTROLS, MODELS 1P74, 1P74, 1P74
AIA-PACK RBC FOLATE
ROCHE ELECSYS FOLATE III, ROCHE ELECSYS RBC FOLATE HEMOLYSING REAGENT, ROCHE ELECSYS FOLATE III CALSET, ROCHE ELECSYS
FOLATE ON THE ACCESS IMMUNOASSAY SYSTEMS, MODEL A14208
ELECSYS RBC FOLATE HEMOLYZED REAGENT
MODIFICATION TO ROCHE ELECSYS FOLATE II IMMUNOASSAY
ROCHE DIAGNOSTICS ELECSYS FOLATE II ASSAY
ABBOTT ARCHITECT FOLATE
ADVIA CENTAUR AND ACS: 180 FOLATE IMMUNOASSAY
VITROS IMMUNODIAGNOSTIC PRODUCTS FOLATE REAGENT PACK 1/2, VITAMIN B12/FOLATE REAGENT PACK 3, PRODUCTS RED CELL FOLATE PA
IMMULITE 2000 FOLIC ACID, MODEL L2KF02, L2KF06
AIA-PACK FOLATE ASSAY
CHIRON DIAGNOSTICS ACS: 180 FOLATE
VITROS IMMUNODIAGNOSTIC PRODUCTS FOLATE REAGENT PACK 1/2, VITROS IMMUNODIAGNOSTIC PRODUCTS VITAMIN B12/FOLATE REAGENT P3
ABBOTT ARCHITECT FOLATE
CEDIA RED BLOOD CELL FOLATE REAGENT PACK, CEDIA FOLATE ASSAY AND ELECSYS FOLATE ASSAY
ABBOTT AXSYM FOLATE
AIA-PACK FOLATE ASSAY
CEDIA RED BLOOD CELL FOLATE (NO BOIL REAGENT PACK)
ACCESS FOLATE ASSAY (MODIFICATION)
RBCFOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM
CEDIA FOLATE (NO BOIL) ASSAY
FOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM, IN VITRO DIAGNOSTIC SYSTEM
IMX FOLATE
RADIAS RED CELL FOLATE IMMUNOASAY
CEDIA(R) FOLATE (NO BOIL) ASSAY
CIBA CORNING ACS FOLATE ASSAY
FOLIC ACID
ACCESS RED BLOOD CELL FOLATE ASSAY
QUANTAPHASE II B12/FOLATE
VISTA FOLATE ASSAY
ACCESS FOLATE ASSAY
RADIAS FOLATE ENZYME IMMUNOASSAY
STRATUS FOLATE FLUOROMETRIC ENZYME-LINKED ASSAY
ACCESS THEOPHYLLINE IMMUNOASSAY REAGENTS
MILENIA FOLIC ACID
CEDIA RED BLOOD CELL FOLATE REAGENT PACK
CIBA CORNING MAGIC LITE FOLATE IMMUNOASSAY
DIAGNON FOLATE 125I RIA KIT
FOLATE RADIOASSAY KIT CA-1562-125
SOLID PHASE SIMUL TRAC VITAMIN B12
VITAMIN B12/FOLATE DUAL RADIOASSAY KITS
QUANTA PHASE VITAMIN B-12/FOLATE RAD

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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