KAE
- Product code
- KAE
- Device name
- Forceps, 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)
- 14
Official FDA classification page: KAE
Classification and pathway per current FDA publications. Data from openFDA (CC0).