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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