Last synced on 25 November 2022 at 11:04 pm

S.M.A.R.T. .018 NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993646
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
11/28/1999
Days to Decision
30 days
Submission Type
Summary

S.M.A.R.T. .018 NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993646
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
11/28/1999
Days to Decision
30 days
Submission Type
Summary