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OMNILINK .018 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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