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: IZD FDA class 1

Probe, Uptake, Nuclear

Radiology

View full classification →

A nuclear uptake probe is a radiation detector used in nuclear medicine to measure the uptake of radioactive tracers in specific organs or tissues, most commonly thyroid gland iodine uptake studies for the evaluation of thyroid function. It is classified as FDA Class 1, the lowest risk designation, requiring only general controls with no premarket notification needed. The product code is IZD, regulated under 21 CFR 892.1320, within the Radiology medical specialty. No special flags apply to this device.

510(k) Clearances

30 matches
K Number
Device Name
DECLIPSESPECT LAPAROSCOPY
DECLIPSESPECT VIEWER
CONFIDENT SURGERY SUITE 300, MODEL CSS300
HANDHELD GAMMA FINDER (HGF)
MODIFICATION TO GAMMA GUIDANCE SYSTEM
C-TRAK AUTOMATIC ANALYZER (NAME CHANGE FROM ONCOPROBE II TO C-TRAK)
NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES
GAMMA GUIDANCE SYSTEM
NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES
NEOPROBE 1000 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES
THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROME
CAPTUS 2000 WEL COUNTER
CAPTUS 500 WELL DETECTOR W/CLINICAL LABOR SOFTWARE
C-TRAK BIOPSY SYSTEM
NEOPROBE PORTABLE RADIOSCOPE DETECTOR
CAPTUS 500
MEDISCINT
THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900
CARDIOSCINT (LEFT VENTRICULAR FUNCTION MONITOR)
ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE
ONCOPROBE II SYSTEM
ACCUSPEC THYROID UPTAKE SYSTEM
ONCOPROBE SYSTEM
NEOPROBE PORTABLE RADIOISOTOPE DETECTOR
ND62T THYROID UPTAKE SYSTEM
THYROID UPTAKE SYSTEM
TOMOMATIC 64
INHAMATIC 33
DIGITAL RADIATION DETECTOR
CARDIAC PROBE

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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