FDA AI Clearance Tracker/K260234

Radiology · 510(k)

MSK Go

Smart Alfa Teknoloji San. Ve Tic. A.S.

Device
MSK Go
Company
Smart Alfa Teknoloji San. Ve Tic. A.S.
Submission number
K260234
Pathway
510(k)
Decision date
May 21, 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.