Last synced on 25 January 2026 at 3:41 am

S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994068
510(k) Type
Special
Applicant
Cordis Corp.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
12/23/1999
Days to Decision
21 days
Submission Type
Summary

S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994068
510(k) Type
Special
Applicant
Cordis Corp.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
12/23/1999
Days to Decision
21 days
Submission Type
Summary