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FDA 510(k) Applications Submitted by ROBERT BOLLINGER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110493
02/22/2011
TANDEMHEART PUMP
CARDIACASSIST INC.
K061369
05/17/2006
TANDEM HEART ESCORT (T.H.E.) CONTROLLER, MODEL 5140-8500
CARDIAC ASSIST, INC.
K082425
08/22/2008
TANDEMHEART TRANSSEPTAL CANNULA- EF 72
CARDIAC ASSIST, INC.
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