Product code KFZ— Anesthesiology
HUMIDIFIER W/ OR W/OUT ADAPTOR
- Classification name
- Humidifier, Non-Direct Patient Interface (Home-Use)
- Device class
- Class 1
- Regulation
- 21 CFR 868.5460
- Advisory panel
- Anesthesiology
- Total cleared
- 20
- First cleared
- Most recent
Market context for product code KFZ
FDA has cleared devices under product code KFZ between 1976 and 1995, filed by 17 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1995
- 1992
- 1990
- 1987
- 1986
- 1985
- 1984
- 1983
- 1981
- 1979
- 1978
- 1976
Top applicants under product code KFZ
Recent clearances under product code KFZ
- K950116 — THERASTEAM PERSONAL STEAM INHALER
- K915603 — VIROTHERM HUMIDIFIER
- K894734 — RHINOTHERM ULTRA 2
- K871661 — WH150 ROOM HUMIDIFIER
- K871189 — SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380
- K862919 — TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER
- K862171 — MP-500 ELECTRONIC NEBULIZER
- K862042 — SH20, SH30 & SH50 ULTRASONIC HUMIDIFIER
- K851220 — SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664
- K852283 — THERMIX INC. NASOTHERM II PERSONAL STEAM MACHINE
- K850711 — INHALATION THERAPY NEBULIZER DEVICE
- K842275 — ULTRASONIC COOL SPRAY HUMIDIFIER
- K840118 — RHINOTHERM
- K831646 — SONIC MIST ULTRASONIC HUMIDIFIER
- K830896 — HUMIDIFIER, WITH OR WITHOUT ADAPTER
- K811161 — HUMIDIFIER W/ OR W/OUT ADAPTOR
- K810335 — RESPIRIZER
- K790966 — ULTRASONIC HUMIDIFIER
- K781591 — NEBULIZER/HUMIDIFIER MODEL EH 147B
- K760341 — HUMIDIFIER, ELECTRONIC (EH147)
Data sourced from openFDA. This site is unofficial and independent of the FDA.