K241593
- 510(k) number
- K241593
- Device name
- BoneMetrics (US)
- Applicant
- Gleamer Sas FR
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-02-05
- Date received
- 2024-06-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K241593.pdf
Official FDA record: K241593
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.