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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Anesthesia Conduction Kit
510(k) Number K780120
Device Name ANESTHESIA TRAY, CAUDAL
Applicant
KENDALL RESEARCH CENTER
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
KENDALL RESEARCH CENTER
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.5140
Classification Product Code
CAZ  
Date Received01/23/1978
Decision Date 02/06/1978
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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