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.

Let the assistant find your predicates

Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

Free to try · every answer cites its records

Product Code: JRQ FDA class 1

Shaker/Stirrer

Clinical Chemistry

View full classification →

The Shaker/Stirrer is a clinical laboratory instrument used to agitate, shake, or stir biological specimens, reagents, or mixtures at controlled speeds to facilitate reactions, ensure homogeneous mixing, and prevent sedimentation during clinical chemistry assay procedures. This device is FDA Class 1, the lowest risk category, requiring only general controls and no premarket notification. It carries product code JRQ and is regulated under 21 CFR 862.2050, within the Clinical Chemistry medical specialty. This device is GMP exempt.

510(k) Clearances

8 matches
K Number
Device Name
MINI-SHAKER
S/P VORTEX MIXER JR.
S/P VORTEX MIXER
SMI MULTI-TUBE VORTEXER
DIMENSIONALL ROTATOR
SHAKER, MODEL SH-510
THERMAJUST CIRCU-TEMP
MICRO-MIX PIPETTE SHAKER

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.

Popular Product Codes

Commonly searched