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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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