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: MSW FDA class 2

System, Test, Thyroglobulin

Immunology

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A Thyroglobulin Test System is an immunoassay-based in vitro diagnostic device used to measure thyroglobulin levels in serum, primarily used to monitor patients with differentiated thyroid cancer for recurrence or metastasis following thyroidectomy. It is FDA Class 2 requiring 510(k) clearance, with product code MSW under 21 CFR 866.6010 in the Immunology specialty. The device is not an implant and is not life-sustaining.

510(k) Clearances

13 matches
K Number
Device Name
Atellica IM Thyroglobulin (Tg)
Access Thyroglobulin
Access Thyroglobulin
Elecsys Tg II
Access Thyroglobulin
ACCESS THYROGLOBULIN REAGENTS ON THE ACCESS IMMUNOASSAY SYSTEMS
BRAHMS DIAGNOSTICA DYNOTEST TG-PLUS
NICHOLS ADVANTAGE THYROGLOB
ACCESS THYROGLOBULIN REAGENTS ON THE ACCESS ANALYZER
NICHOLS CHEMILUMINESCENCE THYROGLOBULIN, MODEL 60-4240
KRONUS OPTIQUANT THYROGLOBULIN KIT
IMMULITE 2000 THYROGLOBULIN MODEL L2KTY
IMMULITE THYROGLOBULIN MODEL LKTY

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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