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FDA 510(k) Applications Submitted by ABBOTT VASCULAR DEVICES
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050501
02/28/2005
MODIFICATION TO: XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM
ABBOTT VASCULAR DEVICES
K052454
09/06/2005
THE EMBOSHIELD EMBOLIC PROTECTION SYSTEM
ABBOTT VASCULAR DEVICES
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