FDA AI Clearance Tracker/K260378

Radiology · 510(k)

Rayvolve

AZmed

Device
Rayvolve
Company
AZmed
Submission number
K260378
Pathway
510(k)
Decision date
May 12, 2026
Specialty (lead panel)
Radiology
Primary product code
QBS

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.