HOI
- Product code
- HOI
- Device name
- Spectacle, Magnifying
- Device class
- Class 1
- 21 CFR
- 21 CFR 886.5840
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 11
Official FDA classification page: HOI
Classification and pathway per current FDA publications. Data from openFDA (CC0).