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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Airway, Esophageal (Obturator)
510(k) Number K761195
Device Name ESOPHAGEAL OBTURATION AIRWAY
Applicant
MCKESSON CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
MCKESSON CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.5650
Classification Product Code
CAO  
Date Received12/06/1976
Decision Date 12/09/1976
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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