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: FQZ FDA class 1

Thermometer, Clinical Color Change

General Hospital

View full classification →

A clinical color change thermometer is a single-use or reusable temperature measurement device that changes color to indicate body temperature, used in routine patient assessment. It is classified as FDA Class 1 (lowest risk), subject to general controls only, and does not require premarket notification. The product code is FQZ, regulated under 21 CFR 880.2900, within the General Hospital medical specialty. No special flags apply to this device.

510(k) Clearances

14 matches
K Number
Device Name
CRY-ACTRACKERCAM
STERI-AID KIT
DEROYAL TECHNOLOGICES, INC. LIQUID CRYSTAL SKIN TEMPERATURE STRIP
POINT CHECKER COLOR STRIP THERMOMETER
FRANKLIN COLLECTOR(R)
TEMPA-DOT CLINICAL THERMOMETER SHEATH
HEALTHCHECK THERM-STRIP
PEE WEE THERMOMETERS
BABY TEMP PACIFIER
MODIFIED TEMPA-DOT THERMOMETER
TEMPO2-I DISPOSABLE THERMOMETERS
THERMOMETER RECAL ADAPTER
THERMOMETER, SINGLE USE, STRIP, TEMPADOT
THERMOMETER, SINGLE USE, STRIP, TEMPADOT

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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