K234076
- 510(k) number
- K234076
- Device name
- iCare ALTIUS CW
- Applicant
- Centervue S.P.A. IT
- Product code
- NFJ — System, Image Management, Ophthalmic
- Decision date
- 2024-08-22
- Date received
- 2023-12-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K234076.pdf
Official FDA record: K234076
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.