Business · 15/08/1994

Cardiac Pacemakers, Inc., Premarket Approval of VENTAKRegister PRxRegister Model 1700 and Model 1705 AICDSUPTM System, Model 2850 PRESCRIPTORSUPTM Programmer and Model 2860 Program Disk

The Food and Drug Administration (FDA) approved the premarket application by Cardiac Pacemakers, Inc. for the VENTAK PRx Model 1700 and Model 1705 AICD TM System, Model 2850 PRESCRIPTOR TM Programmer and Model 2860 Program Disk on June 17, 1994.