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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: MJH FDA class 2

Legionella, Spp., Elisa

Microbiology

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The Legionella Spp. ELISA is an enzyme-linked immunosorbent assay used in clinical microbiology laboratories to detect Legionella species antigens or antibodies in patient specimens such as urine or serum, supporting the diagnosis of Legionnaires' disease and related Legionella infections. Classified as a Class 2 device under 21 CFR 866.3300 within the Microbiology specialty, it requires 510(k) premarket notification. It carries no implant or life-sustaining flags.

510(k) Clearances

10 matches
K Number
Device Name
ImmuView S pneumoniae and L pneumophila Urinary Antigen Test
TRU Legionella
TRU LEGIONELLA
SAS LEGIONELLA TEST, SAS LEGIONELLA DIPSTICK TEST
MODIFICATION TO: BINAX NOW LEGIONELLA URINARY ANTIGEN TEST, #852-000,852-012
LEGIONELLA PNEUMOPHILA IGG/IGM
BARTELS LEGIONELLA URINARY ANTIGEN ELISA TEST
BINAX NOW LEGIONELLA URINARY ANTIGEN TEST MODEL 852-020 AND BINAX NOW LEG IONELLA URINARY ANTIGEN CONTROL KIT MODEL 8522
BINAX LEGIONELLA URINARY ANTIGEN EIA
LEGIONELLA STAT IGG/IGM TEST KIT

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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