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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