510(k) K894969

AEROVENT by Monaghan Medical Corp. — Product Code BZA

K894969 is an FDA 510(k) premarket notification submitted by Monaghan Medical Corp. for the device "AEROVENT". The FDA issued a decision of Substantially Equivalent on October 30, 1989. The device falls under product code BZA (Connector, Airway (Extension)), a Class I device regulated under 21 CFR 868.5810. Monaghan Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 30, 1989
Date Received
August 7, 1989
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