K231662
- 510(k) number
- K231662
- Device name
- Aid-U
- Applicant
- Iaid KR
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-02-08
- Date received
- 2023-06-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K231662.pdf
Official FDA record: K231662
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.