FDA product code KFZ
Humidifier, Non-Direct Patient Interface (Home-Use)
Anesthesiology·Class 1·21 CFR 868.5460
US regulatory classifications
- US Product Code (FDA)
- KFZView Product Code Classification →
- US Risk Class (FDA)
- Class 1
- US Regulation (CFR)
- 21 CFR 868.5460View CFR Regulation →
- Medical specialty
- Anesthesiology
Device characteristics
- GMP exempt
- No
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Not Eligible
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About this record
Humidifier, Non-Direct Patient Interface (Home-Use) is a medical device type in the Anesthesiology specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.
View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.