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: IKW FDA class 1

Utensil, Homemaking

Physical Medicine

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Homemaking Utensils are adapted household tools used in Physical Medicine and occupational therapy to assist patients with limited hand function or mobility in performing daily living tasks such as cooking, cleaning, and household management. It is classified as FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. The product code is IKW, regulated under 21 CFR 890.5050, within the Physical Medicine medical specialty. This device is GMP exempt, indicating it is not subject to full good manufacturing practice requirements.

510(k) Clearances

12 matches
K Number
Device Name
REACHER & DOOR OPENER
CARPET SWEEPER
TURNERS FOR KNOBS
PORTABLE ELECTRIC CAN OPENER
TINY FLEX-GLASS, SET OF 4
JAR HOLDER & OPENER
HOMEMAKING UTENSILS
BK-5371 GAD-19-BOUT PERSONAL MOBIL AID
PRUNING SCISSORS
WEED PULLER & PRUNER
ROLLING PIN
LEVERS, DOOR KNOB, BK-6395

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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