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FDA 510(k) Applications Submitted by MEDTRONIC PERCUSURGE, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K014223
12/26/2001
MODIFICATION TO GUARDWIRE PLUS TEMPORARY OCCLUSION & ASPIRATION SYSTEM
MEDTRONIC PERCUSURGE, INC.
K013913
11/27/2001
PERCUSURGE GUARDWIRE PLUS TEMPORARY OCCLUSION AND ASPIRATION SYSTEM
MEDTRONIC PERCUSURGE, INC.
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