510(k) · Radiology

Heuron ICH

by Heuron Co., Ltd.

Heuron ICH is an AI-enabled medical device from Heuron Co., Ltd. that the U.S. FDA cleared through 510(k) K233247 on May 15, 2024. Its lead review panel is Radiology and its primary product code is QAS (Radiological Computer-Assisted Triage And Notification Software).

See also FDA-cleared AI radiology devices in 2024, all FDA AI clearances in 2024, top radiology AI devices.

Key facts

Submission numberK233247
Pathway510(k)
Date of final decision
Company (FDA list)Heuron Co., Ltd.
Lead review panelRadiology
Primary product codeQAS — Radiological Computer-Assisted Triage And Notification Software
Applicant (openFDA)Heuron Co., Ltd.
Applicant locationSeoul, KR
Device classClass 2
Regulation number21 CFR 892.2080
Decision codeSESE
Submission typeTraditional

Source: FDA AI-Enabled Medical Devices list and openFDA.

What this means

A 510(k) is a premarket submission showing the device is substantially equivalent to a legally marketed predicate device. A cleared 510(k) means FDA agreed with that equivalence. Heuron ICH went through this pathway (K233247).

openFDA lists it as a Class 2 device under 21 CFR 892.2080. Class II devices are moderate risk and are subject to general and special controls.

Product code QAS covers 86 devices on the FDA AI list. By decision date, this device is #55 of 86 under that code. Heuron Co., Ltd. has 2 AI-enabled devices on the list, and the Radiology panel accounts for 1,230 in total.

Being on this list doesn't describe how well the device works clinically. Check the FDA record for its indications for use.

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