QUO

Adjunctive Heart Failure Status Indicator

Product code
QUO
Device name
Adjunctive Heart Failure Status Indicator
Device class
Class 2
21 CFR
21 CFR 870.2200
Medical specialty
Cardiovascular
Marketing pathway
510(K)
510(k) clearances (last 3 years)
3
Summaries archived here
3 (direct download)
510(k) clearances (all years, FDA)
4 (all years; only the last 3 years are listed here)

FDA classification definition

The adjunctive heart failure status indicator is a prescription device based on sensor technology or image data to provide information to an interpreting clinician in detecting heart failure. This device is intended for adjunctive use with other physical vital sign parameters and patient information and is not intended to independently direct therapy.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (3)

Last three years. Most recent: 2025-11-21.

NumberDecision dateApplicantDevice nameSummary
K2512932025-11-21Icardio.AiCardioVisionPDF
K2400132024-09-23Ultromics LimitedEchoGo Heart Failure (2.0)PDF
K2239052023-10-06Avicena, LLCVivio® LVEDP SystemPDF

3 summaries are archived here for direct download.

Official FDA classification page: QUO
Classification and pathway per current FDA publications. Data from openFDA (CC0).