FDA 510(k) Applications Submitted by CARDIOSOLUTIONS INC

FDA 510(k) Number Submission Date Device Name Applicant
K140015 01/02/2014 CARDIOSOLUTIONS DEXTERITY STEERABLE INTRODUCER CARDIOSOLUTIONS INC
K131332 05/09/2013 CARDIOSOLUTIONS PERCU-PRO STEERABLE INTRODUCER CARDIOSOLUTIONS INC
K094048 12/31/2009 PERCUPRO MESSENGER BALLOON CATHETER CARDIOSOLUTIONS INC
K094062 12/31/2009 PERCU-PRO GUIDEWIRE CARDIOSOLUTIONS INC


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