Luminopia— 510(k) K233720

Substantially Equivalent

Luminopia, Inc.

FDA 510(k) clearance K233720 for Luminopia, Substantially Equivalent on 2024-08-08. Applicant: Luminopia, Inc..

Clearance details

Applicant: Luminopia, Inc.
Product code: Code QQU
Advisory panel: Ophthalmic
Date received: 2023-11-21
Decision date: 2024-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cambridge, MA, US

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