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: JWM FDA class 2

System, Tomographic, Nuclear

Radiology

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System, Tomographic, Nuclear is a medical imaging system that uses radioactive tracers and nuclear medicine principles to produce tomographic images of physiological processes and organ function within the body, commonly applied in oncology, cardiology, and neurology. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is JWM, regulated under 21 CFR 892.1310, and falls within the Radiology medical specialty. This device is eligible for third-party review.

510(k) Clearances

17 matches
K Number
Device Name
ICON COMPUTER SYSTEM
D2 SPECTRUM GAMMA CAMERA/CRYSTAL V COMPUTER SYSTEM
ICON
GCA-9300 NUCLEAR TOMOGRAPHY SYSTEM
ADAC MODEL ARC-ST, PC STYLE DATA PROCESSING SYSTEM
ADAC MODEL ARC-5000, GAMMA CAMERA
DIGITAL GAMMA CAMERA GCA 601 E
STARCAM DATA ACQUISITION & PROCESSING SYS H3300C
JUMBO DIGITAL GAMMACAMERA GCA-90B
DIGITAL GAMMA CAMERA GCA 501S
DOT-A, DOT-AR PXP-E, PXP-ER
ECT PROCESSOR
400T ECT SOFTWARE
STAR
STAR
MODUMED MUGX
MODUMED MUGE

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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