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Guidezilla II Guide Extension Catheter; Guidezilla II LONG Guide Extension Catheter

Page Type
Cleared 510(K)
510(k) Number
K163314
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2017
Days to Decision
120 days
Submission Type
Summary

Guidezilla II Guide Extension Catheter; Guidezilla II LONG Guide Extension Catheter

Page Type
Cleared 510(K)
510(k) Number
K163314
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2017
Days to Decision
120 days
Submission Type
Summary