K253930
- 510(k) number
- K253930
- Device name
- Overjet Iris Intelligent Imaging System
- Applicant
- Overjet, Inc. MA · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2026-04-10
- Date received
- 2025-12-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K253930.pdf
Official FDA record: K253930
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.