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: FOX FDA class 1

Stand, Infusion

General Hospital

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The Infusion Stand is a wheeled or floor-mounted pole used in clinical settings to suspend intravenous bags, infusion pumps, and other hanging medical equipment during patient fluid therapy. It is classified as FDA Class 1 (lowest risk) and is subject only to general controls. The product code is FOX, regulated under 21 CFR 880.6990 in the General Hospital specialty.

510(k) Clearances

36 matches
K Number
Device Name
IV STANDS
MEDRAD CONTRAST HOLDER
PORT-A-POLE
HIGH VOLUME I.V. & IRRIGATION TOWER
IV POLE/STAND
IV SHUTTLE
STAND, INFUSION
FLEXSYS MOBILEMATE EQUIPMENT STAND
MOBILE CARE IV STAND
PNEUMATIC IRRIGATION STANDARD
I.V. SKY-HOOK
INTRAVENOUS STAND OR IV STAND
AIV SYSTEMS' IV POLES
HYDRAULIC IV POLE
HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER
DITTMAR POWER LIFTER
CRITICAL CARE I.V. STAND STABILIZING BRACKET
ROD, IRRIGATOR SUPPORTING, TELESCOPING TYPE
POLE, INTRAVENOUS
TRACK AND CARRIER, INTRAVENOUS
INFUSION STAND
STAT-STAND(TM) AND STAT-STAND II(TM)
FREE SPIRIT(TM) I.V. STAND
POLYPOLE
UNICADDY I & II I.V. CONTAINER CADDY IMS POLE MATE
PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD
THE IVY POLE-INTRAVENOUS BOT TREES #1121K & 1221K
INOX IV STAND
STAND, OPERATING ROOM
KARECO INT'L - DOUGLE-HOOK I.V. STAND
IMPACT 901 SERIES PORT-A-WALL
BREWER HEAVE-DUTY I.V. STAND W/FOOT OPERATED PNUEM
HEAVY-DUTY I.V. STAND
MAGUN BASE I.V. POLE
PATIENT PAL I.V. WALKER
CATHETER, SURFLO, I.V.

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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