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: KSQ FDA class 1

Device, Blood Mixing And Blood Weighing

Hematology

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This device is a blood mixing and weighing device used in blood banking to agitate blood bags to prevent clotting during collection and to determine the volume of blood collected by measuring the weight of the blood bag. It is classified as FDA Class 1, the lowest risk category, subject to general controls only. The product code is KSQ, regulated under 21 CFR 864.9195 within the Hematology specialty. No special flags apply.

510(k) Clearances

8 matches
K Number
Device Name
HYCEL ROTOR-MIXER AND/OR MULTI
SEPCOR UNIT COLLECTION MONITOR
PLATELET AGITATOR
MOBILE MATIC AUTOMATIC DONOR SCALE
HEMATIC BLOOD MIXER
ROYCO MODEL 951 CELL MIXER
PLATELET ROTATOR
DONORMATIC (BLOOD COLLECTION DEVICE)

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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