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: KPS FDA class 2

System, Tomography, Computed, Emission

Radiology

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This device is an emission computed tomography system, commonly known as a positron emission tomography (PET) or single-photon emission computed tomography (SPECT) scanner, used to produce functional images of metabolic and physiological activity within the body for diagnostic purposes. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket notification. The product code is KPS, regulated under 21 CFR 892.1200 within the Radiology specialty. This device is eligible for third-party review.

510(k) Clearances

50+ matches
K Number
Device Name
Biograph Vision PET/CT Systems; Biograph mCT PET/CT Systems
Aurora
HeartSee™ Cardiac P.E.T. Processing Software For Myocardial Perfusion and Coronary Flow Reserve (CFR) Version 4
Imaging system of positron emission and X-ray computed tomography (DigitMI 930)
Aurora
uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S)
Hybrid Viewer (00859873006189)
Symbia Pro.specta Q3 (11364751); Symbia Pro.specta X3 (11364752); Symbia Pro.specta X7 (11364753); Symbia Pro.specta VA30A Family
uMI Panorama
uMI Panvivo
Omni Legend
Symbia SPECT and SPECT/CT Systems
NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat
SET-5002
uEXPLORER
Biograph VK10
uMI Panorama
CAREMIBRAIN
cNeuro cPET
Cartesion Prime (PCD-1000A/3) V10.15
Optional Screen Displays for HeartSee Cardiac P.E.T. Processing Software - HeartSee version 4
uMI Panorama
Biograph Vision.X and Biograph Vision.X Edge
Symbia Pro.specta VA20A Family
VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464)
Precision DL
Emory Cardiac Toolbox 4.3
uMI Panorama
Biograph Vision Quadra PET/CT System
DynamicIQ
Omni Legend
EFAI CARDIOSUITE SPECT Myocardial Perfusion Agile Workflows
Radialis PET Camera
SubtlePET
Symbia VA10A Family
MyoSPECT, MyoSpect ES
Discovery MI Gen2
Vereos PET/CT
PET VCAR
Vereos PET/CT
Symbia VA10A Family
HYPER AiR
Cartesion Prime (PCD-1000A/3) V10.8
Optional Screen Display for HeartSee Cardiac P.E.T. Processing Software - HeartSee version 3
HYPER Focus
StarGuide
BBX-PET Scanner
Biograph Vision Quadra PET/CT System
Affinity
SIR-Spheres Microspheres Activity Calculator (SMAC)

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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