K223470
- 510(k) number
- K223470
- Device name
- C50
- Applicant
- Sopro FR
- Product code
- NBL — Light-Induced Fluorescence Caries Detector
- Decision date
- 2023-12-14
- Date received
- 2022-11-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K223470.pdf
Official FDA record: K223470
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.