KYB
- Product code
- KYB
- Device name
- Lens, Guide, Intraocular
- Device class
- Class 1
- 21 CFR
- 21 CFR 886.4300
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 39
Official FDA classification page: KYB
Classification and pathway per current FDA publications. Data from openFDA (CC0).