510(k) K830896
K830896 is an FDA 510(k) premarket notification submitted by Airlife, Inc. for the device "HUMIDIFIER, WITH OR WITHOUT ADAPTER". The FDA issued a decision of Substantially Equivalent on April 18, 1983. The device falls under product code KFZ (Humidifier, Non-Direct Patient Interface (Home-Use)), a Class I device regulated under 21 CFR 868.5460. Airlife, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 18, 1983
- Date Received
- March 21, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Humidifier, Non-Direct Patient Interface (Home-Use)
- Device Class
- Class I
- Regulation Number
- 868.5460
- Review Panel
- AN
- Submission Type