VERVE— 510(k) K232930
Substantially EquivalentOculomotor Technologies
FDA 510(k) clearance K232930 for VERVE, Substantially Equivalent on 2024-06-13. Applicant: Oculomotor Technologies. Device class: 1.
Clearance details
- Applicant
- Oculomotor Technologies
- Product code
- Code SBN
- Device class
- Class 1
- Regulation
- 21 CFR 886.1290
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Princeton, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.