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Steerable Guide Catheter

Page Type
Cleared 510(K)
510(k) Number
K172394
510(k) Type
Special
Applicant
Abbott Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2017
Days to Decision
29 days
Submission Type
Summary

Steerable Guide Catheter

Page Type
Cleared 510(K)
510(k) Number
K172394
510(k) Type
Special
Applicant
Abbott Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2017
Days to Decision
29 days
Submission Type
Summary