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: KXJ FDA class 2

Table, Radiologic

Radiology

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The Radiologic Table is a specialized examination table designed to support patients during X-ray, fluoroscopy, or other radiologic imaging procedures, often incorporating features for table movement and positioning to optimize image acquisition. It is classified as FDA Class 2, indicating moderate risk, and is subject to general controls and special controls, though premarket notification has not been required for this category. The product code is KXJ, regulated under 21 CFR 892.1980, in the Radiology medical specialty. No special flags apply to this device.

510(k) Clearances

31 matches
K Number
Device Name
APOLLO
RADIOGRAPHIC ITT TABLE
XRT 400
IMAGING TABLE
CARBON FIBER COUCH INSERT
INFRARED EXPOSURE HAND SWITCH
SYNCRA TILT OPTION FOR ANGIO DIAGNOST 5
ELECTROPHYSIOLOGY (EP) TABLE EP 2000 SERIES
MODEL COLE TAB-2 TABLE W/MODEL COLE SFD-2 SPOTFILM
CAG-02A
OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400
RADKOR, RF-159
RASTIX X-RAY TABLE
RADKOR KOB-84
UNIVERSAL EXAMINATION TABLE
REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100
OMEGA III ANGIOGRAPHIC TABLE, ROTATION & STEPPER
X-MAT
SHAMPAINE RADI-OP MODEL 1700RC
MEDEX X-RAY TABLE
CHICK/REISON PATIENT EMERG. TROLLEY
SIEMENS SIRESKOP 4
PORTABLE MEDICAL TABLE
DUAL PEDESTAL TABLE
ALLMEC 90/15
TILTING IMAGING TABLE #846T
KOORDINAT 3D
COORDINATUS, HORIZONTAL RADIOGRAPHOC
TELEVIX
CLEARVIEW
KOORDINAT ANGIO

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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