FDA 510(k) Applications Submitted by CARDIO-OPTICS, INC.

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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