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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 K000715
Device Name ENVOY AND VISTA BRITE TIP
Applicant
CORDIS CORP.
14201 N.W. 60TH AVE.
miami lakes,  FL  33014
Applicant Contact dennis s griffin
Correspondent
CORDIS CORP.
14201 N.W. 60TH AVE.
miami lakes,  FL  33014
Correspondent Contact dennis s griffin
Regulation Number870.1250
Classification Product Code
DQY  
Date Received03/02/2000
Decision Date 03/31/2000
Decision substantially equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Special
Reviewed by Third Party No
Combination Product No
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