Last synced on 9 December 2022 at 11:04 pm

LIFESTENT BILIARY STENT SYSTEM, LIFESTENT XL BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130792
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
8/30/2013
Days to Decision
161 days
Submission Type
Summary

LIFESTENT BILIARY STENT SYSTEM, LIFESTENT XL BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130792
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
8/30/2013
Days to Decision
161 days
Submission Type
Summary