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FDA 510(k) Applications Submitted by LARRY BLANKENSHIP
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050808
03/30/2005
CORONARY SINUS ACCESS KIT, MODEL KCS8F-01
CARDIO-OPTICS, INC.
K062340
08/10/2006
CARDIOOPTICS AUGMENTATIVE CARDIAC OPTICAL IMAGING SYSTEM
CARDIO-OPTICS, INC.
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