K240243
- 510(k) number
- K240243
- Device name
- EConsole2
- Applicant
- DRTECH Corporation KR
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-09-23
- Date received
- 2024-01-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K240243.pdf
Official FDA record: K240243
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.