K232440
- 510(k) number
- K232440
- Device name
- Adravision Perio
- Applicant
- Adra Corporation GA · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2023-12-05
- Date received
- 2023-08-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K232440.pdf
Official FDA record: K232440
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.