American Pacemaker Corp.
American Pacemaker Corp. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1982.
Top product codes for American Pacemaker Corp.
Recent clearances by American Pacemaker Corp.
- K821791 — EXTERNAL PULSE GENERATOR - EV4542
- K812807 — APC IMPLANTABLE PACING LEADS
- K812830 — APC IMPLANTABLE PACING LEAD
- K810396 — APC IMPLANTABLE PACING LEAD, TINED #3262
- K810397 — APC IMPLANTABLE PACING LEAD-FLANGE #3260
- K810398 — APC IMPLANTABLE PACING LEAD, MODEL 3266
- K810399 — APC IMPLANTABEL PACING LEAD, MODEL 3264
- K810121 — UNIFOCAL 3
- K800746 — UNIFOCAL VP, MODELS 7501 AND 7502
- K800379 — BIFOCAL 2 8200 SERIES (A,B C,D)
- K791955 — UNIFOCAL 1 UNIPOLAR DEMAND R WAVE
- K792199 — UNIFOCAL 2-UNIPOLAR & BIPOLAR
- K792232 — UNIFOCAL 3-2 MODELS UNIPOLAR & BIPOLAR
- K770328 — PACEMAKER, ANTRIO-VENTRICULAR SEQ.
Data sourced from openFDA. This site is unofficial and independent of the FDA.