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CORDIS PALMAZ CORINTHIAN TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM, CORDIS CRIMPING TOOLS, CORDIS INTRODUCER TUBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992755
510(k) Type
Special
Applicant
Cordis, A Johnson & Johnson Co.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
9/15/1999
Days to Decision
30 days
Submission Type
Summary

CORDIS PALMAZ CORINTHIAN TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM, CORDIS CRIMPING TOOLS, CORDIS INTRODUCER TUBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992755
510(k) Type
Special
Applicant
Cordis, A Johnson & Johnson Co.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
9/15/1999
Days to Decision
30 days
Submission Type
Summary