510(k) K811708

UNIVERSAL ADAPTER SYSTEM-U/ADAPIT by Airlife, Inc. — Product Code BZA

K811708 is an FDA 510(k) premarket notification submitted by Airlife, Inc. for the device "UNIVERSAL ADAPTER SYSTEM-U/ADAPIT". The FDA issued a decision of Substantially Equivalent on July 1, 1981. The device falls under product code BZA (Connector, Airway (Extension)), a Class I device regulated under 21 CFR 868.5810. Airlife, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 1, 1981
Date Received
June 16, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Connector, Airway (Extension)
Device Class
Class I
Regulation Number
868.5810
Review Panel
AN
Submission Type