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: IXJ FDA class 1

Grid, Radiographic

Radiology

View full classification →

A radiographic grid is a device consisting of alternating strips of radiation-absorbing and radiation-transmitting materials placed between the patient and the imaging receptor to reduce scatter radiation and improve radiographic image contrast. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is IXJ, regulated under 21 CFR 892.1910, within the Radiology medical specialty.

510(k) Clearances

15 matches
K Number
Device Name
MITAYA ALUMINUM INTERSPACED X-RAY GRID
FIBRE INTERSPACED X-RAY GRID
RADIOGRAPHIC GRID
HIGH TRANSMISSION CELLULAR (HTC) GRIDS 18X24 CM & 24X30 CM SIZES
SK S-RAY GRIDS
JPI X-RAY GRID
GRIDGIL
X-RAY GRID (RADIOLOGICAL GRID)
SOYEE ALUMINUM INTERSPACED X-RAY GRID
JPI ALUMINUM INTERSPACED X-RAY GRID
KODAK EKTASCAN SP CASSETTE
RADIOGRAPHIC GRID
GRID/RADIOGRAPHIC
TBX MEDICAL X-RAY TABLE
AOR X-RAY ALIGMENT PAD

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.

Popular Product Codes

Commonly searched