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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 K982770
Device Name 6F ENVOY GUIDING CATHETER
Applicant
CORDIS CORP.
14000 N.W. 57TH COURT
MIAMI LAKES,  FL  33014
Applicant Contact MARTINE D SCHNEIDER
Correspondent
CORDIS CORP.
14000 N.W. 57TH COURT
MIAMI LAKES,  FL  33014
Correspondent Contact MARTINE D SCHNEIDER
Regulation Number870.1250
Classification Product Code
DQY  
Date Received07/23/1998
Decision Date 08/18/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
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