HOW
- Product code
- HOW
- Device name
- Drum, Opticokinetic
- Device class
- Class 1
- 21 CFR
- 21 CFR 886.1200
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K) Exempt
- Flag
- GMP exempt
- 510(k) clearances (last 3 years)
- 1
Official FDA classification page: HOW
Classification and pathway per current FDA publications. Data from openFDA (CC0).