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RX HERCULINK ELITE BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K053454
510(k) Type
Traditional
Applicant
GUIDANT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
3/6/2006
Days to Decision
87 days
Submission Type
Summary

RX HERCULINK ELITE BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K053454
510(k) Type
Traditional
Applicant
GUIDANT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
3/6/2006
Days to Decision
87 days
Submission Type
Summary