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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