510(k) · Radiology

EchoSolv AS

by Echo IQ Ltd

EchoSolv AS is an AI-enabled medical device from Echo IQ Ltd that the U.S. FDA cleared through 510(k) K241245 on October 4, 2024. Its lead review panel is Radiology and its primary product code is POK (Computer-Assisted Diagnostic Software For Lesions Suspicious For Cancer).

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

Key facts

Submission numberK241245
Pathway510(k)
Date of final decision
Company (FDA list)Echo IQ Ltd
Lead review panelRadiology
Primary product codePOK — Computer-Assisted Diagnostic Software For Lesions Suspicious For Cancer
Applicant (openFDA)Echo IQ, Ltd.
Applicant locationSydney, AU
Device classClass 2
Regulation number21 CFR 892.2060
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. EchoSolv AS went through this pathway (K241245).

openFDA lists it as a Class 2 device under 21 CFR 892.2060. Class II devices are moderate risk and are subject to general and special controls.

Product code POK covers 22 devices on the FDA AI list. By decision date, this device is #12 of 22 under that code. Echo IQ Ltd has 1 AI-enabled device 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.

Similar devices (product code POK)