FDA 510(k) Applications Submitted by DAVID D BROOKE

FDA 510(k) Number Submission Date Device Name Applicant
K090521 02/26/2009 DIAMONDBACK 360 DBX CARDIOVASCULAR SYSTEMS, INC.
K083139 10/23/2008 VIPERSPHERE PTA BALLOON CATHETER CARDIOVASCULAR SYSTEMS, INC.
K081944 07/08/2008 MODIFICATION TO DIAMONDBACK 360 DEGREE ORBITAL ATHERECTOMY SYSTEM CARDIO SYSTEMS, INC.
K082981 10/06/2008 DIAMONDBACK 360 DEGREE ORBITAL ATHERECTOMY SYSTEM WITH VIPERSLIDE LUBRICANT CARDIOVASCULAR SYSTEMS, INC.


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