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: IMJ FDA class 2

Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

Physical Medicine

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Shortwave Diathermy for Applying Therapeutic Deep Heat is a Physical Medicine device that uses high-frequency electromagnetic energy in the shortwave radiofrequency range to generate deep tissue heating within muscles and joints, used to reduce pain, relieve muscle spasm, and increase local circulation. It is classified as FDA Class 2, representing moderate risk, meaning it requires a 510(k) premarket notification demonstrating substantial equivalence to a predicate device before marketing. The product code is IMJ, regulated under 21 CFR 890.5290, within the Physical Medicine medical specialty. This device is eligible for third party review, meaning the 510(k) submission may be reviewed by an FDA-accredited third party organization.

510(k) Clearances

43 matches
K Number
Device Name
Curapuls 670
Reprieve by RegenesisTM
BTL-703
ViaTherm BOOST
ProMedTek Model C1400 Shortwave Diathermy Device
ThermoPro
Megapulse III Shortwave Diathermy
THERMOPULSE
SW-THERM
BIOFUSIONARY BEBE
BTL ELITE
INTELECT SWD 100, MODEL 1600; SENIOR SOLUTIONS SHORTWAVE DIATHERMY, MODEL 1601
AUTO THERM 390, MODEL ME 390
SELITHERM, MODEL C100
SW-180 SHORTWAVE THERAPY UNIT
AUTO*THERM 395, MODEL ME 395
SELICOR, MODELS A100 & D100
MEGAPULSE II
ULTRATHERM (908)
THEE THERMASTIM
VASOTHERM
MAGNATHERM MODEL 1000 SS
TRU-SOUND ULTRASOUND THERAPY UNIT
SOUNDTEK MODEL UT-4700
MODEL 2060 W/6 CM(2) & MODEL 2100 W/10 CM(2) TRANS
THE BIO-TEK UW-II
ULTRATHERM 808 I
NEMECTROSON MODEL 2
MEDTRON TYPE P-300 ULTRASONIC THERAPY UNIT
RICH-MAR RM-2000 ULTRASOUND PHYSICAL THERAPY DEVIC
RICH-MAR RM 2002 ULTRASOUND PHYSICAL THERAPY DEVIC
CURAMED 402 DIATHERMY UNIT
CURAPULS 419 DIATHERMY UNIT
THERMO SHORTWAVE DIATHERMY
CURAMED 402
THERMOPULS E
ULTRAMED 11S601
MEGA PULSE THERAPY UNIT
SIEMENS ULTRATHERM 708
PULSED AND CONTINUOUS SHORTWAVE APPAR.
SHORTWAVE THERAPY APPAR. CURAMED 401
SHORTWAVE DIATHERMY MODEL 802
MAGNATHERM 2000

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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