510(k) K953400

GUEDEL AIRWAY by Mallinckrodt Medical — Product Code CAE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 24, 1995
Date Received
July 20, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Airway, Oropharyngeal, Anesthesiology
Device Class
Class I
Regulation Number
868.5110
Review Panel
AN
Submission Type