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BARD E LUMINEXX BILIARY STENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063532
510(k) Type
Traditional
Applicant
BARD PERIPHERAL VASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
5/30/2008
Days to Decision
555 days
Submission Type
Summary

BARD E LUMINEXX BILIARY STENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063532
510(k) Type
Traditional
Applicant
BARD PERIPHERAL VASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
5/30/2008
Days to Decision
555 days
Submission Type
Summary