QTO
2022-08-12
Digital Visual Acuity Test
FDA product code QTO · 1 cleared devices
Class 1
Ophthalmic
- Regulation
- 21 CFR 886.1150
- Review panel
- OP
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2022-08-12 – 2022-08-12
A Digital visual acuity testing system is intended as an aid in the assessment of visual acuity in patients.
No matching devices.
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