K260032
- 510(k) number
- K260032
- Device name
- Morph
- Applicant
- BeauBrain Healthcare, Inc. KR
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2026-05-13
- Date received
- 2026-01-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K260032.pdf
Official FDA record: K260032
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.