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: IOL FDA class 1

Treadmill, Powered

Physical Medicine

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A Powered Treadmill is a motorized walking and running device used in Physical Medicine for cardiovascular rehabilitation, gait training, and exercise therapy, with a motor-driven belt providing a controlled walking surface at adjustable speeds and inclines. 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 IOL, regulated under 21 CFR 890.5380, within the Physical Medicine medical specialty.

510(k) Clearances

43 matches
K Number
Device Name
PARKER MODEL PM
PARKER MODEL PE
TRACKMASTER
RTM REHABILITATION TREADMILL, MODEL #945-200
MANSFIELD CARDIAC ASSIST MODEL 940(TM) IAB
TA620 TREADMILL CONTROLLER
T600 TREADMILL
MEDTRACK TREADMILL
ORBITER(TM) TREADMILL
AQUATREX UNDERWATER TREADMILL SYSTEM
PACER R 9 TREADMILL
STARTRAC
MODIFIED Q-SERIES OF TREADMILLS
MODEL Q55XT POWERED TREADMILL
MODIFIED Q50 MEDICAL TREADMILL
Q50 MEDICAL TREADMILL
R1596 POWERED EXERCISE EQUIPMENT
BATTLE CREEK BOARDWALKER ELECTRIC TREADMILL
BATTLE CREEK DIGI-TRACKER ELCTRIC TREADMILL
CAMBRIDGE MODEL XT1000
TMX-C1/C2 TRADMILL CONTROLLER ACCESS.
TMX-80 TREADMILL
TMX-70 TREADMILL
TREADMILL E-17
LAUF-ERGOTEST JUNIOR
LAUF-ERGOTEST
ROAD RUNNER ELECTRIC TREADMILL
VASCULAR LABORATORY TREADMILL VT1
PROGRAM. TREADMILL CONTROLLER #645
Q65 MEDICAL TREADMILL
POWERED TREADMILL
QUINTON Q55 MEDICAL TREADMILL
SAS EDUCATIONAL CHART
TELETRED GAIT ANALYSIS SYSTEM
SERIES 1800 EXERCISE TREADMILL
TREADMILL MODEL 3060
AP-1 AUTO PROGRAMMER
CARDIO-EXERCISE TREADMILL 550
TREADMILL STRESS EXERCISE SYSTEM
POWERED TREADMILL (30/ST)
POWERED TREADMILL (20/ST)
TREADMILL, DIAGNOSTIC
TREADMILL (TMS-300)

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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