Radiology · 510(k) · 2026
Automated Aortic Stenosis Software (AutoAS)
GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC. Cleared by FDA on 27 March 2026 under submission K254161, product code POK (computer-assisted diagnostic software for lesions suspicious for cancer). What FDA's record says, in FDA's words.
Device record · K254161
- Device. Automated Aortic Stenosis Software (AutoAS)DEVICE
- Company. GE Medical Systems Ultrasound & Primary Care Diagnostics, LLCCOMPANY
- Decision. 27 March 2026, 510(k), substantially equivalent (traditional review); received 22 December 2025DECISION
- Panel. RadiologyPANEL
- Product code. POK, Computer-Assisted Diagnostic Software For Lesions Suspicious For CancerCODE
- Regulation. 21 CFR 892.2060, Class IIREG
- Source. FDA database entry · decision document (15 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.
AutoAS is a software application intended to assist medical professionals in the assessment of moderate/severe aortic stenosis (AS). The software uses an artificial intelligence (AI) algorithm to process previously acquired two-dimensional transthoracic echocardiography (2D-TTE) images to provide a suggestion of moderate/severe aortic stenosis along with an associated confidence metric that can be a diagnostic aid to a physician in a point of care or similar setting in determining if further evaluation is needed, including whether a full echocardiogram (2D, Doppler) needs to be performed. The results of AutoAS are not intended to be used on a stand-alone basis for clinical decision making and are not intended to supplement or replace a full echocardiographic examination. AutoAS results, along with the obtained ultrasound images, must be reviewed by a qualified physician. The AutoAS product is not intended to be used on patients who have prosthetic valves and/or have had prior valve repair or replacement. AutoAS software is indicated for use in adult patients and is intended to be an accessory to compatible ultrasound systems in environments where healthcare is provided.
The product code's definition, from FDA's classification record. Assist users in characterizing lesions identified on acquired medical images
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.
- Modalities namedultrasound
- Mentionsa diagnostic claim
- Mentionsadult patients
Adverse-event reports in MAUDE, by product code
As of , MAUDE held 1 report filed against devices carrying product code POK. 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:
15 January 2021 · Malfunction · QUANTX · report MW5098869
QUANTX SOFTWARE MAY ENTER INTO AN ERROR STATE IN WHICH MEDICAL IMAGES DISPLAYED TO THE USER ARE FROZEN IN PLACE. QUANTX SOFTWARE VERSION (B)(4) ENTER INTO AN ERROR STATE IN WHICH ONE VIEWPORT IS FROZEN IN PLACE. WHEN THIS ERROR OCCURS, QUANTX STOPS RESPONDING TO USER INPUTS TO MODIFY THE DISPLAY OF THE FROZEN IMAGE. THIS ERROR STATE IS REACHED THROUGH A SPECIFIC SEQUENCE OF KEYSTROKES AND MOUSE ACTIONS. ONCE THE ONE IMAGE IS FROZEN IN A VIEWPORT IT REMAINS FROZEN. IT WILL ALSO REMAIN FROZEN IF […]
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 POK, in Radiology, from GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC, or cleared in 2026. 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.