KAI
- Product code
- KAI
- Device name
- Mirror, Ent
- Device class
- Class 1
- 21 CFR
- 21 CFR 874.4420
- Medical specialty
- Ear, Nose, Throat
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 9
Official FDA classification page: KAI
Classification and pathway per current FDA publications. Data from openFDA (CC0).