FDA AI Clearance Tracker/K260780

Radiology · 510(k)

HeartFocus

Deski

Device
HeartFocus
Company
Deski
Submission number
K260780
Pathway
510(k)
Decision date
Jun 3, 2026
Specialty (lead panel)
Radiology
Primary product code
QJU

Source: U.S. FDA AI-Enabled Medical Devices list. The FDA says the list is not comprehensive. Confirm details on the FDA's own record.