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: JTQ FDA class 1

Bath, Incubators/Water, All

Microbiology

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Bath, Incubators/Water, All is a laboratory instrument category encompassing water baths and incubators used to maintain specimens, culture media, or reagents at controlled temperatures required for microbiological and biochemical analyses. It is classified as FDA Class 1, the lowest risk category, subject to general controls only. The product code is JTQ, regulated under 21 CFR 866.2540, and falls within the Microbiology medical specialty. This device is exempt from Good Manufacturing Practice (GMP) regulations.

510(k) Clearances

12 matches
K Number
Device Name
WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER
PLATE INCUBATOR
ANHYDRIC INCUBATORS, CULTURE INCUBATOR
C.A.T. REAGENT KIT
AUTOMATED ELISA READER LBI 300
LBI-100 37DEGREES INCUBATOR
WATER BATH
FORMA CH/P GAS PROCESSOR
TITERTEK MICROPLATE INCUBATOR
SPOR-O-THERM
TEMPTRONIC 100 WATER BATH
BLOOD BANK DRI-BATH

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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