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Steerable Guide Catheter

Page Type
Cleared 510(K)
510(k) Number
K161985
510(k) Type
Special
Applicant
ABBOTT VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2016
Days to Decision
19 days
Submission Type
Summary

Steerable Guide Catheter

Page Type
Cleared 510(K)
510(k) Number
K161985
510(k) Type
Special
Applicant
ABBOTT VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2016
Days to Decision
19 days
Submission Type
Summary