Visibly Digital Acuity Product— 510(k) K220090
Substantially EquivalentVisibly, Inc.
FDA 510(k) clearance K220090 for Visibly Digital Acuity Product, Substantially Equivalent on 2022-08-12. Applicant: Visibly, Inc.. Device class: 1.
Clearance details
- Applicant
- Visibly, Inc.
- Product code
- Code QTO
- Device class
- Class 1
- Regulation
- 21 CFR 886.1150
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chicago, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.