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FDA PRODUCT CODE · CLASS II

QUOAdjunctive Heart Failure Status Indicator

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.

DEVICE CLASS
Class II
REGULATION
21 CFR 870.2200
MEDICAL SPECIALTY
Cardiovascular
REVIEW PANEL
CV
ImplantLife-sustainingGMP-exemptThird-party review eligible
2
510(K)/PMA CLEARANCES
510k: 2
0
RECALL ENTRIES

Recent clearances

K251293Icardio.Ai · 510k2025-11-21
K240013Ultromics Limited · 510k2024-09-23

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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