Visibly Digital Acuity Product— 510(k) K220090

Substantially Equivalent

Visibly, Inc.

FDA 510(k) clearance K220090 for Visibly Digital Acuity Product, Substantially Equivalent on 2022-08-12. Applicant: Visibly, Inc..

Clearance details

Applicant: Visibly, Inc.
Product code: Code QTO
Advisory panel: Ophthalmic
Date received: 2022-01-11
Decision date: 2022-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

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