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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Tubing, Pump, Cardiopulmonary Bypass
510(k) Number K810924
Device Name MEDRAD HIGH PRESSURE CONECTING TUBE
Applicant
Medrad, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Medrad, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.4390
Classification Product Code
DWE  
Date Received04/06/1981
Decision Date 04/17/1981
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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