EchoGo Heart Failure (2.0) is an AI-enabled medical device from Ultromics Limited that the U.S. FDA cleared through 510(k) K240013 on September 23, 2024. Its lead review panel is Cardiovascular and its primary product code is QUO (Adjunctive Heart Failure Status Indicator).
See also FDA-cleared AI cardiovascular devices in 2024, all FDA AI clearances in 2024, top cardiovascular AI devices.
Key facts
| Submission number | K240013 |
|---|---|
| Pathway | 510(k) |
| Date of final decision | |
| Company (FDA list) | Ultromics Limited |
| Lead review panel | Cardiovascular |
| Primary product code | QUO — Adjunctive Heart Failure Status Indicator |
| Applicant (openFDA) | Ultromics Limited |
| Applicant location | Oxford, GB |
| Device class | Class 2 |
| Regulation number | 21 CFR 870.2200 |
| Decision code | SESE |
| Submission type | Traditional |
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. EchoGo Heart Failure (2.0) went through this pathway (K240013).
openFDA lists it as a Class 2 device under 21 CFR 870.2200. Class II devices are moderate risk and are subject to general and special controls.
Product code QUO covers 3 devices on the FDA AI list. By decision date, this device is #2 of 3 under that code. Ultromics Limited has 3 AI-enabled devices on the list, and the Cardiovascular panel accounts for 154 in total.
Being on this list doesn't describe how well the device works clinically. Check the FDA record for its indications for use.