Last synced on 20 December 2024 at 11:05 pm

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
K011039
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
5/8/2001
Days to Decision
33 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
K011039
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
5/8/2001
Days to Decision
33 days
Submission Type
Summary