K240610
- 510(k) number
- K240610
- Device name
- deepLive
- Applicant
- Damae Medical FR
- Product code
- NQQ — System, Imaging, Optical Coherence Tomography (Oct)
- Decision date
- 2024-07-09
- Date received
- 2024-03-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K240610.pdf
Official FDA record: K240610
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.