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: QFO FDA class 2

Zika Virus Serological Reagents

Microbiology

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The Zika Virus Serological Reagents consist of antigens and antisera for the presumptive clinical diagnosis of Zika virus infection in human clinical specimens from individuals with signs and symptoms consistent with Zika virus infection and/or epidemiological risk factors, used in conjunction with other clinical and laboratory findings. It is classified as FDA Class 2, requiring 510(k) premarket notification under regulation 866.3935 in the Microbiology specialty. The product code is QFO. It is not an implant and is not life-sustaining.

510(k) Clearances

4 matches
K Number
Device Name
DPP Zika IgM System, DPP Zika IgM System Control Pack, and DPP Micro Reader
LIAISON XL Zika Capture IgM II and LIAISON XL Zika Capture IgM II Control Set
ADVIA Centaur Zika test, ADVIA Centaur Zika Ab (100 tests), ADVIA Centaur Zika IgM (50 tests), ADVIA Centaur Zika Ab Quality Control, ADVIA Centaur Zika IgM Quality Control
ZIKV Detect 2.0 IgM Capture ELISA

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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