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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 K874412
Device Name THE PROTECTOR
Applicant
TRI JON, INC.
810 W. MITCHELL #421
P.O. BOX 13928
ARLINGTON,  TX  76013
Applicant Contact JOHNNY COOPER
Correspondent
TRI JON, INC.
810 W. MITCHELL #421
P.O. BOX 13928
ARLINGTON,  TX  76013
Correspondent Contact JOHNNY COOPER
Regulation Number868.5110
Classification Product Code
CAE  
Date Received10/28/1987
Decision Date 02/12/1988
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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