American Pacemaker Corp. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
American Pacemaker Corp. has 14 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1977 to 1982.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Jul 06, 1982
EXTERNAL PULSE GENERATOR - EV4542
Cardiovascular
19d
Cleared
Jan 18, 1982
APC IMPLANTABLE PACING LEADS
Cardiovascular
104d
Cleared
Jan 18, 1982
APC IMPLANTABLE PACING LEAD
Cardiovascular
102d
Cleared
May 15, 1981
APC IMPLANTABLE PACING LEAD, TINED #3262
Cardiovascular
86d
Cleared
May 15, 1981
APC IMPLANTABLE PACING LEAD-FLANGE #3260
Cardiovascular
86d
Cleared
May 15, 1981
APC IMPLANTABLE PACING LEAD, MODEL 3266
Cardiovascular
86d
Cleared
May 15, 1981
APC IMPLANTABEL PACING LEAD, MODEL 3264
Cardiovascular
86d
Cleared
Feb 23, 1981
UNIFOCAL 3
Radiology
35d
Cleared
Dec 16, 1980
UNIFOCAL VP, MODELS 7501 AND 7502
Cardiovascular
257d
Cleared
Sep 26, 1980
BIFOCAL 2 8200 SERIES (A,B C,D)
Cardiovascular
217d
Cleared
Nov 27, 1979
UNIFOCAL 1 UNIPOLAR DEMAND R WAVE
Cardiovascular
57d
Cleared
Nov 27, 1979
UNIFOCAL 2-UNIPOLAR & BIPOLAR
Cardiovascular
26d
Cleared
Nov 27, 1979
UNIFOCAL 3-2 MODELS UNIPOLAR & BIPOLAR
Cardiovascular
22d
Cleared
Feb 28, 1977
PACEMAKER, ANTRIO-VENTRICULAR SEQ.
Cardiovascular
11d