Luminopia One— 510(k) DEN210005

Unknown

Luminopia, Inc.

FDA 510(k) clearance DEN210005 for Luminopia One, Unknown on 2021-10-20. Applicant: Luminopia, Inc..

Clearance details

Applicant: Luminopia, Inc.
Product code: Code QQU
Advisory panel: Ophthalmic
Date received: 2021-03-01
Decision date: 2021-10-20
Decision: Unknown
Clearance type: Direct
Location: Cambridge, MA, US

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