HeartFocus

Deski · K260780 · 2026-06-03

HeartFocus is an AI-enabled medical device from Deski, listed by FDA (510(k), K260780) with a decision date of 2026-06-03. Review panel: Radiology.

FDA submission numberK260780
Pathway510(k)
CompanyDeski
Review panel (specialty)Radiology
FDA decision date2026-06-03
DecisionSubstantially Equivalent
Product codeQJU
ClassificationImage Acquisition And/Or Optimization Guided By Artificial Intelligence
Device class2
Regulation number892.2100
Review time (calendar days)85
Applicant countryFR

Official FDA database record · FDA AI-enabled device list

All Radiology AI devices · Full device index

Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.