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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Filter, Blood, Cardiopulmonary Bypass, Arterial Line
510(k) Number K813131
Device Name INTERFACE ARTERIAL BLOOD FILTER
Applicant
Medical, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Medical, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.4260
Classification Product Code
DTM  
Date Received11/05/1981
Decision Date 11/27/1981
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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