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: IRT FDA class 2

Pad, Heating, Powered

Physical Medicine

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A powered heating pad is an electrically operated pad that provides controlled therapeutic heat to localized body areas for relief of muscle pain, stiffness, and related musculoskeletal conditions. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is IRT, regulated under 21 CFR 890.5740, within the Physical Medicine medical specialty.

510(k) Clearances

41 matches
K Number
Device Name
bite away neo
Bite Away
Heated Eye Pad
AVACEN 100
FIR HEAT THERAPHY SYSYEMS
BIO-MAT 2000
PT-PAC PORTABLE HEATING PAD
LI'S ITCH STOPPER
HEALTH O METER ELECTRIC HEATING PADS MODELS EHP2, EHP3
HEALTH O METER ELECTRIC HEATING PAD W/MASSAGE MODEL EHP4
PES HOT/COLD COMPRESS
FEMININE HEAT WRAP
ELASTOPLAST HEAT PLASTER
ARTHRITIC HEAT WRAP
MOSIST HEAT PAD WITH AUTOMATIC OFF
MOIST HEAT PAD
KING SIZE HEAT PAD
THERMODYN
PNEUMATHERM
SPORTS HEAT WRAP
DUNLAP HEAT PAD
SANDBOX I, SANDBOX II, SANDBOX JR.
INFRASSAGE MASSAGER
BCS NO. 1, BODY CARE SYSTEM
PORT-O-HEAT, MODEL 0100
THERMO-BODY-WRAP SYSTEM
HUCHEL BODYLINER
THERMOWRAP, A/K/A/, THERMAL WRAP
FORMOSTAR
SOLEX THERAPEUTIC PAD
THERMO TRIM
MUSCLE MINDER: HEAT WRAP W/ HOT + COLD PACK
THERMOPHORE ELECTRIC FOMENTATION UNIT
HYDRO-THERO PAD
HP-20, 30, 40, 50 & 60
MICROPAD
PASSIVE HEAT PADS
DELUXE HEAT WRAP/COLD WRAP
THERMAL CONDITIONING SYSTEM
GILLETTE HEAT WRAP
THERATHERM

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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