VERVE— 510(k) K232930

Substantially Equivalent

Oculomotor Technologies

FDA 510(k) clearance K232930 for VERVE, Substantially Equivalent on 2024-06-13. Applicant: Oculomotor Technologies.

Clearance details

Applicant: Oculomotor Technologies
Product code: Code SBN
Advisory panel: Ophthalmic
Date received: 2023-09-20
Decision date: 2024-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Princeton, NJ, US

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