FDA 510(k) Applications Submitted by CARDIAC ASSIST, MAQUET CARDIOVASCULAR LLC

FDA 510(k) Number Submission Date Device Name Applicant
K112327 08/12/2011 SENSATION(TM) PLUS 8FR. 50CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES CARDIAC ASSIST, MAQUET CARDIOVASCULAR LLC
K112372 08/17/2011 CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP CARDIAC ASSIST, MAQUET CARDIOVASCULAR LLC


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