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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Oxygenator, Cardiopulmonary Bypass
510(k) Number K854045
Device Name MEMBRANE OXYGENATING SYS ADULT BMOS-7 & BMOS-3 PED
Applicant
American Bentley
17502 Armstrong Ave.
Irvine,  CA  92714
Applicant Contact DONALD A RAIBLE
Correspondent
American Bentley
17502 Armstrong Ave.
Irvine,  CA  92714
Correspondent Contact DONALD A RAIBLE
Regulation Number870.4350
Classification Product Code
DTZ  
Date Received10/02/1985
Decision Date 12/16/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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