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RX HERCULINK PLUS BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K010684
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
4/12/2001
Days to Decision
35 days
Submission Type
Summary

RX HERCULINK PLUS BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K010684
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
4/12/2001
Days to Decision
35 days
Submission Type
Summary