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OMNILINK .018 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K033834
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
1/2/2004
Days to Decision
23 days
Submission Type
Summary

OMNILINK .018 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K033834
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
1/2/2004
Days to Decision
23 days
Submission Type
Summary