FDA AI Clearance Tracker/K254120

Radiology · 510(k)

SubtleHD-CT (1.x)

Subtle Medical, Inc.

Device
SubtleHD-CT (1.x)
Company
Subtle Medical, Inc.
Submission number
K254120
Pathway
510(k)
Decision date
May 15, 2026
Specialty (lead panel)
Radiology
Primary product code
QIH

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.