K231678
- 510(k) number
- K231678
- Device name
- Overjet Periapical Radiolucency Assist
- Applicant
- Overjet, Inc. MA · US
- Product code
- MYN — Analyzer, Medical Image
- Decision date
- 2023-09-21
- Date received
- 2023-06-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.1 MB · U.S. public domain
Also available from FDA: K231678.pdf
Official FDA record: K231678
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.