K232085
- 510(k) number
- K232085
- Device name
- DVAS (DVAS-M, DVAS-W)
- Applicant
- Genoray Co., Ltd. KR
- Product code
- EHD — Unit, X-Ray, Extraoral With Timer
- Decision date
- 2023-12-08
- Date received
- 2023-07-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K232085.pdf
Official FDA record: K232085
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.