K232930
- 510(k) number
- K232930
- Device name
- VERVE
- Applicant
- Oculomotor Technologies NJ · US
- Product code
- SBN — Digital Therapy Device For Convergence Insufficiency
- Decision date
- 2024-06-13
- Date received
- 2023-09-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 1.5 MB · U.S. public domain
Also available from FDA: K232930.pdf
Official FDA record: K232930
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.