FDA 510(k) Applications Submitted by MIKE BILLIG

FDA 510(k) Number Submission Date Device Name Applicant
K982419 07/13/1998 HEART-LIFT BALLOON POSITIONER CARDIOTHORACIC SYSTEMS, INC.
K983135 09/08/1998 BLOWER/MISTER CARDIOTHORACIC SYSTEMS, INC.
K983270 09/17/1998 VOYAGER QUAD CANNULA CARDIOTHORACIC SYSTEMS, INC.


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