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: IYZ FDA class 1

Bed, Scanning, Nuclear

Radiology

View full classification →

A nuclear scanning bed is a patient support table designed for use with nuclear medicine imaging systems, positioning and transporting the patient through the detector field during whole-body or regional scintigraphic scanning. It is classified as FDA Class 1, reflecting the lowest level of regulatory oversight, with only general controls required. The product code is IYZ, regulated under 21 CFR 892.1350, within the Radiology medical specialty. No special flags apply to this device.

510(k) Clearances

12 matches
K Number
Device Name
MULTIPLE ACCESSORY TO GAMMA CAMERAS
SPECT TABLE, MODEL #056-760
XYZ CRANK IMAGING TABLE
CARDIAC SPECT PALLET
ECT CARBON FIBER PALLET, MODIFICATION
XY IMAGING TABLE
E-Z LIFT CRANK IMAGING TABLE
E-Z LIFT IMAGING TABLE WITH FOOT PUMP
XYZ IMAGING TABLE WITH FOOT PUMP
SCANNING COT
ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL
QRSYSTEMS H.D. NUCLEAR IMAGING 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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