K252922
- 510(k) number
- K252922
- Device name
- Neosoma Brain Mets
- Applicant
- Neosoma, Inc. MA · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-12-17
- Date received
- 2025-09-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K252922.pdf
Official FDA record: K252922
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.