510(k) · Radiology

LOGIQ E10s, LOGIQ Fortis

by GE Medical Systems Ultrasound and Primary Care Diagnostic,

LOGIQ E10s, LOGIQ Fortis is an AI-enabled medical device from GE Medical Systems Ultrasound and Primary Care Diagnostic, that the U.S. FDA cleared through 510(k) K231989 on November 7, 2023. Its lead review panel is Radiology and its primary product code is IYN (System, Imaging, Pulsed Doppler, Ultrasonic).

See also FDA-cleared AI radiology devices in 2023, all FDA AI clearances in 2023, top radiology AI devices.

Key facts

Submission numberK231989
Pathway510(k)
Date of final decision
Company (FDA list)GE Medical Systems Ultrasound and Primary Care Diagnostic,
Lead review panelRadiology
Primary product codeIYN — System, Imaging, Pulsed Doppler, Ultrasonic
Applicant (openFDA)Ge Medical Systems Ultrasound and Primary Care Diagnostic,
Applicant locationWauwatosa, WI, US
Device classClass 2
Regulation number21 CFR 892.1550
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. LOGIQ E10s, LOGIQ Fortis went through this pathway (K231989).

openFDA lists it as a Class 2 device under 21 CFR 892.1550. Class II devices are moderate risk and are subject to general and special controls.

Product code IYN covers 124 devices on the FDA AI list. By decision date, this device is #54 of 124 under that code. GE Medical Systems Ultrasound and Primary Care Diagnostic, 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.

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