K242203
- 510(k) number
- K242203
- Device name
- BriefCase-Quantification
- Applicant
- Aidoc Medical , Ltd. IL
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-11-22
- Date received
- 2024-07-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K242203.pdf
Official FDA record: K242203
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.