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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Connector, Airway (Extension)
510(k) Number K884374
Device Name E.T. PUFFER
Applicant
KALAJIAN ENT.
P.O. BOX 30401
LONG BEACH,  CA  90853
Applicant Contact W KALAYJIAN
Correspondent
KALAJIAN ENT.
P.O. BOX 30401
LONG BEACH,  CA  90853
Correspondent Contact W KALAYJIAN
Regulation Number868.5810
Classification Product Code
BZA  
Date Received10/18/1988
Decision Date 11/23/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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