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: IKX FDA class 1

Aid, Transfer

Physical Medicine

View full classification →

A Transfer Aid is a device used in Physical Medicine and occupational therapy to assist caregivers and patients in safely moving individuals with limited mobility from one surface to another, such as from a bed to a wheelchair or a chair to a vehicle, reducing injury risk for both patient and caregiver. 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 IKX, 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

18 matches
K Number
Device Name
TRICYCLES
WALL GRAB BARS 98130-98136
TUB TRANSFER BENCH BK6481
BATH TUB SAFETY BAR
BOARD TO TRANSFER PARALYZED PATIENT FROM
CHAIR OR BED LEG EXTENDERS
BATH TUB SEAT & BATH BOARD
SHOWER STOOL W/HANDLES
DISC-O-AID
BATHTUB TRANSFER BENCH
BK-6111 HI-D TRANSFER BOARD
TRANSFER BENCH
TRANSFER AIDS
GRAB BARS
TAYLOR PATIENT TRANSFER BOARD
BOARD, TRANSFER, FENDER
GRAB BAR
SLIDING BOARD

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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