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: INW FDA class 1

Table, Mechanical

Physical Medicine

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A Mechanical Therapy Table is a manually adjustable clinical treatment table used in Physical Medicine that incorporates mechanical adjustment mechanisms for height or section positioning, providing a versatile platform for patient examination, rehabilitation exercises, and therapeutic interventions. 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 INW, regulated under 21 CFR 890.3750, within the Physical Medicine medical specialty.

510(k) Clearances

35 matches
K Number
Device Name
JAMES LECKEY FREE STANDER
JAMES LECKEY PRONE STANDER
EURO TECH PLATINUM CHIROPRACTIC TABLE
EURO TECH MARQUISE CHIROPRACTIC TABLE
TUMBLE FORMS JUNIOR TRISTANDER
ECONOMY HI-LOW WORK TABLE (MANUAL) MODEL 3405
ECO. HI-LOW TREATMENT TABLES VARIOUS MODEL NUMBERS
ECONOMY HI-LOW MAT TABLE #4110 THRU 4117
PROFESSIONAL & ECONMY TILT TABLE 9500 9520
TREATMENT TABLES, MANUALLY ACTIVATED
DESKS
ABLE GENERATION DESK
TUMBLE FORMS TRISTANDER
EXTENDO-BAC TABLE
TITAN ZODIAC ADJUSTING TABLE
TITAN HERCULES ADJUSTING TABLE
GRASP (GRIGG-RUSSEL AIR SUPPORT PILLOW)
THE WAVERLY WEDGE(TM) INFLATABLE AIR CUSHION
REFLUX BED
MODEL #510/515 GENERAL TRANSPORT STRETCHER
MODEL #520/525 ED/RECOVERY STRETCHER
E653 OBLONG ABDUCTION BLOCK
E655 ADJUSTABLE ABDUCTION BLOCK W/HIP STABILIZER
E613 PAIR OF SUPPORT BLOCKS
E65 35 PRONE STANDER
MECHANICAL TABLES AND ACCESSORIES
ZENITH TRAVELER CHIROPRACTIC TABLE
HEFFINGTON KNEE REST
SCHOOLTABLE
R1436,R1697,R1699,R1564,R1216,R1214,R854 & R1213
OB TILT TABLE
ACRATRAC R
MECHANICAL TABLE
TRITON
MILLER TABLE

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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