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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Airway, Oropharyngeal, Anesthesiology
510(k) Number K883593
Device Name #400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY
Applicant
Ecolab, Inc.
Ecolab Center
St. Paul,  MN  55102
Applicant Contact ANN M OXFORD
Correspondent
Ecolab, Inc.
Ecolab Center
St. Paul,  MN  55102
Correspondent Contact ANN M OXFORD
Regulation Number868.5110
Classification Product Code
CAE  
Date Received08/23/1988
Decision Date 09/30/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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