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Xcess Guiding Catheter

Page Type
Cleared 510(K)
510(k) Number
K180797
510(k) Type
Traditional
Applicant
Curatia Medical Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2018
Days to Decision
262 days
Submission Type
Summary

Xcess Guiding Catheter

Page Type
Cleared 510(K)
510(k) Number
K180797
510(k) Type
Traditional
Applicant
Curatia Medical Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2018
Days to Decision
262 days
Submission Type
Summary