K233590
- 510(k) number
- K233590
- Device name
- Overjet Charting Assist
- Applicant
- Overjet, Inc. MA · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-02-23
- Date received
- 2023-11-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K233590.pdf
Official FDA record: K233590
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.