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: JTX FDA class 1

Transport Systems, Anaerobic

Microbiology

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Transport Systems, Anaerobic are specimen collection and transport systems designed to preserve anaerobic microorganisms by maintaining an oxygen-free environment from sample collection through laboratory receipt, ensuring viability of obligate anaerobes for culture and identification. It is classified as FDA Class 1, posing the lowest risk and subject to general controls only. The product code is JTX, regulated under 21 CFR 866.2900, and falls within the Microbiology medical specialty. This device is eligible for third-party review.

510(k) Clearances

8 matches
K Number
Device Name
ANAEROBIC ACCU-CULSHURE(TM)
ACUSON V328 AND C5432 TRANSDUCERS
ACCU-CULSHURE TM
BIO-BAG ENVIRONMENTAL CHAMBER (A & B)
STANDARDIZE TGCL & TGCH
ANASWAB
PRE-DUCED SURGI-SWAB & TRANSPORTER TUBE
SPECIMEN COLLECTOR, ANAEROBIC

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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