K253899
- 510(k) number
- K253899
- Device name
- 3D-Anywhere
- Applicant
- Provect.AI CA · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2026-07-09
- Date received
- 2025-12-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K253899.pdf
Official FDA record: K253899
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.