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: DGE FDA class 2

Igd, Rhodamine, Antigen, Antiserum, Control

Immunology

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The IgD Rhodamine Antigen, Antiserum, and Control is a rhodamine-labeled fluorescent immunological reagent designed to detect IgD immunoglobulins, a class expressed primarily on the surface of mature B lymphocytes. It is classified as FDA Class 2, requiring 510(k) premarket notification, and is regulated under 21 CFR 866.5510 within the Immunology specialty. The device is eligible for third-party 510(k) review.

510(k) Clearances

2 matches
K Number
Device Name
OPUS FERRITIN TEST SYSTEM
STRATUS IGE FLUOROMETRIC ENZYME IMMUNOASSAY

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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