510(k) K830896

HUMIDIFIER, WITH OR WITHOUT ADAPTER by Airlife, Inc. — Product Code KFZ

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