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FDA 510(k) Applications Submitted by KEVIN DRISCO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K014205
12/21/2001
MODIFICATION TO BRIDGE SELF-EXPANDING BILIARY STENT DELIVERY SYSTEM (BRIDGE SE)
MEDTRONIC AVE, INC.
K973138
08/21/1997
SPIROCARD
QRS DIAGNOSTIC, LLC.
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