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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 K954595
Device Name CORDIS BRITE TIP SHEATH INTRODUCER
Original Applicant
CORDIS CORP.
14201 n.w. 60th ave.
miami lakes,  FL  33014
Original Contact tamara yount
Regulation Number870.1340
Classification Product Code
DYB  
Date Received10/03/1995
Decision Date 12/28/1995
Decision substantially equivalent (SE)
Classification Advisory Committee Cardiovascular
Review Advisory Committee Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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