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: INM FDA class 1

Chair, With Casters

Physical Medicine

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A Chair with Casters is a mobile seating device used in Physical Medicine and clinical environments that incorporates caster wheels to allow repositioning of the patient or chair without lifting, supporting patient comfort and clinical workflow in rehabilitation and hospital settings. 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 INM, regulated under 21 CFR 890.3100, within the Physical Medicine medical specialty.

510(k) Clearances

35 matches
K Number
Device Name
NISSIN PEDIATRIC SERIES WHEELCHAIR
STRYKER 5050 STRECHAIR
CAREMOR CLINER
RECLINING GERI CHAIRS W/CASTERS & LAP TRAY
BENCHES
CHAIRS
ELD-ARONDAK CHAIR
ELD-ARONDAK CHAIR
STONEHEART ROLLER AID
KAYE SCOOT-ABOUT, MODEL SB1
SHOWER CHAIRS
DOLOMITE ROLLATOR
AMBULATOR
RIFTON MOR219 19 & RIFTON MOR225 25
DUKKI
ZIGGY MEDICHAIR
SHOWER CHAIR
MULTI-CARE CHAIR
MECHANICAL WALKER
KOOYCHAIR (PEDIATRIC)
MERIVAARA GERIATRIC CHAIR
AHLBERGS KOMBI I & KOMBI II MOBILE TRANSFER CHAIRS
MEDICAL CHAIR, MULTIPURPOSE TAST SUPPORT
ALPHA PUSH KART
WALK & ROLL
OSLO ARMCHAIR
PORTABLE TRANSIT CHAIR
OB TRIPP TRANSPORT CHAIR
OB TRIPP TRANSPORT CHAIR
PEOPLE MOVER
ESCORT
FOLDING ROLL-ABOUT CHAIR
FOLDING SHOWER-COMMODE CHAIR
ROLLCHAIR, ORTHO BUCKET SEAT
CHAIRS WITH CASTORS

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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