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: CEE FDA class 2

Radioimmunoassay, Thyroxine-Binding Globulin

Clinical Chemistry

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The Thyroxine-Binding Globulin Radioimmunoassay is a clinical chemistry device that uses radiolabeled immunoassay methods to measure the concentration of thyroxine-binding globulin (TBG) in serum, used in the interpretation of thyroid hormone levels and investigation of abnormal total thyroid hormone results due to TBG abnormalities. It is classified as FDA Class 2 (moderate risk), though it is exempt from 510(k) premarket notification. The product code is CEE, regulated under 21 CFR 862.1685, within the Clinical Chemistry medical specialty. No special flags apply to this device.

510(k) Clearances

25 matches
K Number
Device Name
AMERLITE TBG ASSAY
ACCESS THYROID UPTAKE ASSAY
IMMULITE(TM) T-UPTAKE
MICROZYME THYROID UPTAKE ENZYME IMMUNOASSAY KIT
DELFIA TBG KIT
ENZYMUN TEST(R) TBK
AMERLITE TBG ASSAY, LAN.0005/1005 240/144 TEST KIT
T-UPTAKE MICROASSAY
FIAGEN TBG TIME-RESOLVED FLUOROIMMUNOASSAY KIT
TECHNICON RA(R) ANALYTE (TBG) (30 C AND 37 C)
ENZYMUN TEST TBG
TIPSEP-TBG ASSAY
TBG RIA
THYROXINE-BINDING GLOBULIN RADIOUMMU
VENTREZYME T4U IMMUNOASSAY T4U
ENDAB THYROID UPTAKE
TBG DIAGNOSTIC KIT
IN-VITRO TBG RADIOIMMUNOASSAY TEST
RIA PHASE TBG
GLOBULIN TEST, HUMAN THYROXINE BINDING
125 I-T3 UPTAKE REAGENT
STIKSEP-T3 KIT
THYROID BINDING GLOBULIN
SPINSEP-TBG
PROCEDURE, RA, THYROXINE BINDING PROTEIN

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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