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AXIOS Stent and Electrocautery Enhanced Delivery System

Page Type
Cleared 510(K)
510(k) Number
K192043
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2019
Days to Decision
26 days
Submission Type
Summary

AXIOS Stent and Electrocautery Enhanced Delivery System

Page Type
Cleared 510(K)
510(k) Number
K192043
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2019
Days to Decision
26 days
Submission Type
Summary