Zdrowie i gospodarka · 06/05/1994

Pace Medical, Inc.; Premarket Approval of the Model 4553 MICRO-PACESUPTM Dual-Chamber, DDD, Temporary Cardiac Pacemaker

The Food and Drug Administration (FDA) approved the premarket application of Pace Medical, Inc. for its Model 4553 MICRO-PACE TM Dual-Chamber, DDD, Temporary Cardiac Pacemaker on March 10, 1994.