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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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