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GUIDEZILLA GUIDE EXTENSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K123765
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2013
Days to Decision
102 days
Submission Type
Summary

GUIDEZILLA GUIDE EXTENSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K123765
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2013
Days to Decision
102 days
Submission Type
Summary