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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 K820045
Device Name CARDIOVASCULAR DEVICES
Applicant
Bentley Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Bentley Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.4260
Classification Product Code
DTM  
Date Received01/07/1982
Decision Date 01/29/1982
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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