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: IXQ FDA class 2

Table, Radiographic, Stationary Top

Radiology

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A stationary-top radiographic table is a patient support table with a fixed, non-tilting tabletop designed to position patients for radiographic examinations, providing a stable, radiolucent surface for X-ray imaging procedures. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is IXQ, regulated under 21 CFR 892.1980, within the Radiology medical specialty.

510(k) Clearances

27 matches
K Number
Device Name
CARBON FIBER CONFORMAL COUCH TOP
MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300
MED-TEC HAND GRIP
EURO, SCST, SCCFT ATLAS RADIOLOGIC TABLES
OCTOPAQUE UNIVERSAL
ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE
DIAL-A-RAD PORTA RAD TABLE
R-MADE HEAD/ARM SUPPORT
BUCKY TABLE BK-12
CLINITRON C-10
MILITARY RADIOGRAPHIC FLAT TABLE, CAT # T-9130
ECONOMY C-ARM TABLE, MODEL # 056-005
RADIOGRAPHIC TRANSPORT, TRAUMA MODEL 056-230, 235
LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS
SUPER SPEED POTTER-BUCKY (ESO5-110 & 220)
RADKOR TS10-B
REI-38 RADIOGRAPHIC TABLE
ALTAIREX BUCKY/CASSETTE TRAY COMBINATION
HI-LO ELEVATOR FLAT TABLE
ITT INTERGRATED TABLE AND TUBESTAND
TABLE RADIOGRAPHIC FIXED
XMC-S TUBESTAND XMT-S TABLE XMH-NTWALL
XMA INTEGRATED TABLE
CAROLINA X-RAY CO. SIMPLAFLOAT TABLE
PHIPIOLOGICAL SYNCHRONIZER PART#205
PLURIX B; RADIOGRAPHIC TABLE
PLURIX C; RADIOGRAPHIC 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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