Last synced on 2 December 2022 at 11:04 pm

XPAND BALLOON-EXPANDABLE TRANSHEPATIC BILIARY STENT SYSTEM, MODELS 20587, 20588, 20589, 20603, 20604, 20605

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041962
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/2004
Days to Decision
72 days
Submission Type
Summary

XPAND BALLOON-EXPANDABLE TRANSHEPATIC BILIARY STENT SYSTEM, MODELS 20587, 20588, 20589, 20603, 20604, 20605

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041962
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/2004
Days to Decision
72 days
Submission Type
Summary