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PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K041796
510(k) Type
Special
Applicant
CORDIS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
8/3/2004
Days to Decision
32 days
Submission Type
Summary

PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K041796
510(k) Type
Special
Applicant
CORDIS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
8/3/2004
Days to Decision
32 days
Submission Type
Summary