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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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