KFZ
- Product code
- KFZ
- Device name
- Humidifier, Non-Direct Patient Interface (Home-Use)
- Device class
- Class 1
- 21 CFR
- 21 CFR 868.5460
- Medical specialty
- Anesthesiology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 20 (all years; only the last 3 years are listed here)
Official FDA classification page: KFZ
Classification and pathway per current FDA publications. Data from openFDA (CC0).