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QuikPass Catheter

Page Type
Cleared 510(K)
510(k) Number
K214106
510(k) Type
Traditional
Applicant
Traverse Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2022
Days to Decision
30 days
Submission Type
Summary

QuikPass Catheter

Page Type
Cleared 510(K)
510(k) Number
K214106
510(k) Type
Traditional
Applicant
Traverse Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2022
Days to Decision
30 days
Submission Type
Summary