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CES INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K965181
510(k) Type
Traditional
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1997
Days to Decision
87 days
Submission Type
Summary

CES INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K965181
510(k) Type
Traditional
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1997
Days to Decision
87 days
Submission Type
Summary