510(k) K861540

DISPOSABLE BERMAN AND GUEDEL AIRWAYS by Dryden Corp. — Product Code CAE

K861540 is an FDA 510(k) premarket notification submitted by Dryden Corp. for the device "DISPOSABLE BERMAN AND GUEDEL AIRWAYS". The FDA issued a decision of Substantially Equivalent on May 2, 1986. The device falls under product code CAE (Airway, Oropharyngeal, Anesthesiology), a Class I device regulated under 21 CFR 868.5110. Dryden Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 2, 1986
Date Received
April 24, 1986
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