VERVE
FDA 510(k) clearance K232930 · decided 2024-06-13
Clearance details
- K-number
- K232930
- Device name
- VERVE
- Applicant
- Oculomotor Technologies
- Decision
- Substantially Equivalent
- Date received
- 2023-09-20
- Decision date
- 2024-06-13
- Days to decision
- 267 days
- Clearance type
- Traditional
- Product code
- SBN
- Device class
- 1
- Regulation number
- 886.1290
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Princeton, NJ, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.