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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name catheter, percutaneous
510(k) Number K811971
Device Name CORDIS DUCOR PTR SYSTEM
Applicant
CORDIS CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
CORDIS CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number870.1250
Classification Product Code
DQY  
Date Received07/10/1981
Decision Date 08/13/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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