FDA AI Clearance Tracker/K260032

Radiology · 510(k)

Morph

BeauBrain Healthcare, Inc.

Device
Morph
Company
BeauBrain Healthcare, Inc.
Submission number
K260032
Pathway
510(k)
Decision date
May 13, 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.