510(k) K851699

COOK PACEMAKER CORP. 332T BIPOLAR CARDIAC PULSE GE by Cook Pacemaker Corp. — Product Code DXY

K851699 is an FDA 510(k) premarket notification submitted by Cook Pacemaker Corp. for the device "COOK PACEMAKER CORP. 332T BIPOLAR CARDIAC PULSE GE". The FDA issued a decision of Substantially Equivalent on May 16, 1985. The device falls under product code DXY (Implantable Pacemaker Pulse-Generator), a Class III device regulated under 21 CFR 870.3610. Cook Pacemaker Corp. has at least 10 other 510(k) clearances on record.