KBE
- Product code
- KBE
- Device name
- Snare, Nasal
- Device class
- Class 1
- 21 CFR
- 21 CFR 874.4420
- Medical specialty
- Ear, Nose, Throat
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: KBE
Classification and pathway per current FDA publications. Data from openFDA (CC0).