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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name introducer, catheter
510(k) Number K945524
Device Name CORDIS INTRODUCING CATHETER
Original Applicant
CORDIS CORP.
14201 n.w. 60th ave.
miami lakes,  FL  33014
Original Contact kevin macdonald
Regulation Number870.1340
Classification Product Code
DYB  
Date Received11/10/1994
Decision Date 04/26/1995
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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