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MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032530
510(k) Type
Special
Applicant
GUIDANT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/23/2003
Days to Decision
69 days
Submission Type
Summary

MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032530
510(k) Type
Special
Applicant
GUIDANT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/23/2003
Days to Decision
69 days
Submission Type
Summary