Radiology · 510(k) · 2023
LOGIQ E10
GE Medical Systems Ultrasound and Primary care Diagnostics,. Cleared by FDA on 7 November 2023 under submission K231966, product code IYN (system, imaging, pulsed doppler, ultrasonic). What FDA's record says, in FDA's words.
Device record · K231966
- Device. LOGIQ E10DEVICE
- Company. GE Medical Systems Ultrasound and Primary care Diagnostics,COMPANY
- Decision. 7 November 2023, 510(k), substantially equivalent (traditional review); received 3 July 2023DECISION
- Panel. RadiologyPANEL
- Product code. IYN, System, Imaging, Pulsed Doppler, UltrasonicCODE
- Regulation. 21 CFR 892.1550, Class IIREG
- Source. FDA database entry · decision document (10 pages)SOURCE
Retrieved · the fields above are FDA's; the statement below was copied from the decision document on that day.
What FDA cleared it for
The Indications for Use statement, verbatim, from the decision document.
Technology: mm wide (keyboard), 991 mm deep and 1300 mm high that provides digital acquisition, processing and display capability. The user interface includes a computer keyboard, specialized controls, 12-inch high- resolution color touch screen and 23.8-inch High Contrast LED LCD monitor. LOGIQ E10 is intended for use by a qualified physician for ultras ound evaluation of Fetal / Obstetrics; Abdominal (inc luding Renal, Gynecology/Pelvic); Pe diatric; Small Organ (B reast, T estes, Thyroid); Neonatal Cephalic; Adult Cepha lic; Cardiac ( Adult and P ediatric); Peripheral Vascular; Musculo -skeletal Conventional an d Superficial; Urology (including P rostate); Transrec tal; Trans vaginal; Transesophageal and Intraoperative (Abdominal and Vascular). Modes of operation include: B, M, P W Doppler, CW Doppler, Color Doppler, Color M Doppler, Power Doppler, Harmonic Ima ging, Coded Pulse, 3D/4D Imaging mode, Elastogra phy, Shear Wave Elas tography, Attenuation Imaging an d Combined modes: B/ M, B/Color, B/ PWD, B/Color/PWD, B/Power/PWD. The LOG IQ E10 is intended to be used in a hospital or medical clinic. Th e LOGIQ E10 employs the same fundamental scientific technology as its predicate device(s). Determination of
What the statement says
Pattern matches on the Indications for Use text. Each line is a fact that the text contains the words, not a finding about the device.
- Mentionsadult patients
- Mentionspediatric patients
Adverse-event reports in MAUDE, by product code
As of , MAUDE held 2,748 reports filed against devices carrying product code IYN. That code is shared by every device of this type, not this device alone, and MAUDE reports are submitted by manufacturers, facilities and the public without FDA verification. The latest reports, in the reporter’s words:
30 September 2026 · Malfunction · ACUSON Origin Ultrasound System · Siemens Medical Solutions USA, Inc. · report 3023245-2026-00096
30 September 2026 · Malfunction · ACUSON Sequoia Ultrasound System · Siemens Medical Solutions USA, Inc. · report 3023245-2026-00097
30 September 2026 · Malfunction · AFFINITI 30 · Philips Ultrasound, Inc · report 3019216-2026-100325
30 September 2026 · Injury · EPIQ 5G · Philips Ultrasound, Inc · report 3019216-2026-100326
29 September 2026 · Malfunction · ACUSON Juniper · Siemens Medical Solutions USA, Inc. · report 3023245-2026-00091
One of the patient exams performed on the Juniper system displays an "Unarchived" error message and they are unable to send this study to PACS. All other exams performed before are after this one are transferring over to the PACS as expected without any errors. The problem occurred after a Breast study was completed and the user tried to send it over to the network PACS. TSE worked with the customer and she confirmed that the problem cannot be reproduced, as it only is affecting this one exam. […]
Where this fits
This page is a record, not medical advice and not a safety rating. It copies FDA's fields and FDA's statement, and lists what the statement's text mentions. Read the labeling before relying on any of it.
More devices under product code IYN, in Radiology, from GE Medical Systems Ultrasound and Primary care Diagnostics,, or cleared in 2023. The whole record is at FDA AI-enabled medical devices.
A device's authorized use is a sentence the record can be read against. What Apodicta does on a medical record is that reading: every line of a note, a claim or a report proved to its source or held, before it renders.