Last synced on 25 January 2026 at 3:41 am

SMART NITINOL STENT ENDOSCOPIC BILIARY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030409
510(k) Type
Special
Applicant
Cordis Corp.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
3/10/2003
Days to Decision
31 days
Submission Type
Summary

SMART NITINOL STENT ENDOSCOPIC BILIARY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030409
510(k) Type
Special
Applicant
Cordis Corp.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
3/10/2003
Days to Decision
31 days
Submission Type
Summary