K251730
- 510(k) number
- K251730
- Device name
- LIA Console (542-7)
- Applicant
- Leadoptik, Inc. CA · US
- Product code
- NQQ — System, Imaging, Optical Coherence Tomography (Oct)
- Decision date
- 2025-12-19
- Date received
- 2025-06-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K251730.pdf
Official FDA record: K251730
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.