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: JTT FDA class 2

Susceptibility Test Powders, Antimicrobial

Microbiology

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Susceptibility Test Powders, Antimicrobial are accurately weighed or quantified antimicrobial agent powders used to prepare standardized stock solutions for broth microdilution or agar dilution susceptibility testing, allowing determination of minimum inhibitory concentrations (MICs) for bacterial isolates. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is JTT, regulated under 21 CFR 866.1640, and falls within the Microbiology medical specialty. This device is eligible for third-party review.

510(k) Clearances

14 matches
K Number
Device Name
SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES WITH SPARFLOXACIN
PASCO MIC AND MIC/ID PANELS
BACTEC PYRAZINAMIDE SUSCEPTIBILITY TEST
MODIFIED IMIPENEM SUSCEPTIBILITY POWDER
CIPRO (TM) DIAGNOSTIC POWDER
NORFLOXACIN SUSCEPTIBILITY POWDER
IMIPENEM 10 MCG SENSITIVITY DISCS
GEN DIAGNOSTICS' IMIPENEM 10 MCG SUSCEPTIBITY DISK
IMIPENEM SUSCEPTIBILITY POWDER
IMIPENEM 10 MCG SENSI-DISC,CAT. # 31644/31645
AZLIN AZLOCILIN SODIUM-DIAG. REAGENT
MOXALACTAM
ANTITUBERCULOUS DRUGS (SIRE)
MEZLIN DIAGNOSTIC REAGENT

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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