QTO
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Digital Visual Acuity Test
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1150
- Medical specialty
- Ophthalmic
- FDA definition
- A Digital visual acuity testing system is intended as an aid in the assessment of visual acuity in patients.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| Visibly Digital Acuity Product (K220090) | Visibly, Inc. | 2022-08-12 |
Track QTO automatically
Every clearance here is in the API, with alerts when new ones post.