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Cobra Catheter System

Page Type
Cleared 510(K)
510(k) Number
K223891
510(k) Type
Traditional
Applicant
Endovascular Engineering
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2023
Days to Decision
50 days
Submission Type
Summary

Cobra Catheter System

Page Type
Cleared 510(K)
510(k) Number
K223891
510(k) Type
Traditional
Applicant
Endovascular Engineering
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2023
Days to Decision
50 days
Submission Type
Summary