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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Ventilator, Emergency, Manual (Resuscitator)
510(k) Number K871147
Device Name MODIFIED CPREVIVER
Applicant
AUGERSCOPE, INC.
12860 AM FERNANDO RD.
SYLMAR,  CA  91342 -3797
Applicant Contact HOWARD G BENTLEY
Correspondent
AUGERSCOPE, INC.
12860 AM FERNANDO RD.
SYLMAR,  CA  91342 -3797
Correspondent Contact HOWARD G BENTLEY
Regulation Number868.5915
Classification Product Code
BTM  
Date Received03/12/1987
Decision Date 04/20/1987
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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