FDA 510(k) Applications Submitted by DEBBIE COGAN

FDA 510(k) Number Submission Date Device Name Applicant
K020701 03/04/2002 SYNCRUS INTERNAL CARDIOVERSION SYSTEM GUIDANT CORPORATION, CARDIAC SURGERY
K062458 08/23/2006 ETHMOID SINUS SPACER ACCLARENT, INC.
K052454 09/06/2005 THE EMBOSHIELD EMBOLIC PROTECTION SYSTEM ABBOTT VASCULAR DEVICES
K063078 10/10/2006 MICROENDOSCOPE ACCLARENT, INC.
K024071 12/10/2002 GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM GUIDANT CORPORATION, CARDIAC SURGERY


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