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MODIFICATION TO RX HERCULINK ELITE BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063481
510(k) Type
Traditional
Applicant
ABBOTT VASCULAR INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
9/14/2007
Days to Decision
301 days
Submission Type
Summary

MODIFICATION TO RX HERCULINK ELITE BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063481
510(k) Type
Traditional
Applicant
ABBOTT VASCULAR INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
9/14/2007
Days to Decision
301 days
Submission Type
Summary