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MODIFICATION TO CORDIS BRITE TIP CATHETER SHEATH INTRODUCER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K983023
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1998
Days to Decision
31 days
Submission Type
Summary

MODIFICATION TO CORDIS BRITE TIP CATHETER SHEATH INTRODUCER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K983023
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1998
Days to Decision
31 days
Submission Type
Summary