K240003
- 510(k) number
- K240003
- Device name
- Velmeni for Dentists (V4D)
- Applicant
- Velmeni, Inc. CA · US
- Product code
- MYN — Analyzer, Medical Image
- Decision date
- 2024-08-30
- Date received
- 2024-01-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K240003.pdf
Official FDA record: K240003
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.