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: NFJ FDA class 2

System, Image Management, Ophthalmic

Radiology

View full classification →

The System, Image Management, Ophthalmic (product code NFJ) is a radiology/ophthalmic device system used to manage, organize, archive, and retrieve ophthalmic diagnostic images within a clinical or hospital environment. It is classified as an FDA Class 2 device within the Radiology specialty, requiring 510(k) premarket clearance. No specific regulation number has been assigned to this product code. The device is not flagged as an implant or life-sustaining device.

510(k) Clearances

50+ matches
K Number
Device Name
iCare ALTIUS CW
IMAGEnet6 Ophthalmic Data System
CALLISTO eye
Harmony
CALLISTO eye
Altris IMS
Excelsior
FORUM
RetinAI Discovery
Harmony Referral System
CellChek 20 rc
Image Quality Analyzer (IQA)
ImageSPECTRUM
Glaucoma Module
CONTINUUM PACS
OVision Imaging System
Huvitz Imaging System
KOWA VK-2s
Afina
Retina Workplace
Harmony
Image Filing Software NAVIS-EX
Welch Allyn RetinaVue Network REF 901108 PACS Medical Image System
CALLISTO eye
Ophthalmic Software Platform RX
IMAGEnet 6 Ophthalmic Data System
Retina Workplace
AXIS Image Management System
Huvitz Imaging System
OptosAdvance 4.0 Software
Synergy ODM
Retina Workplace
IRIS INTELLIGENT RETINAL IMAGING SYSTEM
FORUM GLAUCOMA WORKPLACE
EyeSuite Imaging
IMAGENET 5 PC SOFTWARE SYSTEM
SYNERGY ODM
FORUM GLAUCOMA WORKPLACE
EXCELSIOR
CALLISTO EYE
FORUM FORUM ARCHIVE FORUM ARCHIVE & VIEWER FORUM ASSIST MATCH
OPTOS ADVANCE
CARA
OIS SYMPHONY IMAGE MANAGMENT SYSTEM
SYNERGY
MATCHEDFLICKER
FORUM
IMAGE STORAGE SYSTEM, MODEL KSS-400
IMAGENET PROFESSIONAL PC SOFTWARE SYSTEM OR IMAGENET PROFESSIONAL, OR IMAGENET PRO, OR DIGITAL IMAGING SOFTWARE FOR
IP SYSTEM, OCULAB IP, OPTOMIZE IP, RETASURE IP

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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