K243989
- 510(k) number
- K243989
- Device name
- Second Opinion® 3D
- Applicant
- Pearl, Inc. CA · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-05-23
- Date received
- 2024-12-26
- 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: K243989.pdf
Official FDA record: K243989
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.