FDA product code QTO
Digital Visual Acuity Test
Ophthalmic·Class 1·21 CFR 886.1150
US regulatory classifications
- US Product Code (FDA)
- QTOView Product Code Classification →
- US Risk Class (FDA)
- Class 1
- US Regulation (CFR)
- 21 CFR 886.1150View CFR Regulation →
- Medical specialty
- Ophthalmic
Device characteristics
- GMP exempt
- No
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Not Eligible
Definition
A Digital visual acuity testing system is intended as an aid in the assessment of visual acuity in patients.
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About this record
Digital Visual Acuity Test is a medical device type in the Ophthalmic specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.
View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.