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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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