K231225
- 510(k) number
- K231225
- Device name
- EConsole1
- Applicant
- DRTECH Corporation KR
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2023-10-18
- Date received
- 2023-04-28
- 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: K231225.pdf
Official FDA record: K231225
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.