K252195
- 510(k) number
- K252195
- Device name
- ARTICOR planner
- Applicant
- Artiness S.R.L IT
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2026-03-27
- Date received
- 2025-07-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K252195.pdf
Official FDA record: K252195
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.