K232456
- 510(k) number
- K232456
- Device name
- RW-1
- Applicant
- Mediott, Inc. JP
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2025-08-11
- Date received
- 2023-08-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.2 MB · U.S. public domain
Also available from FDA: K232456.pdf
Official FDA record: K232456
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.