Siemens-Pacesetter, Inc. - FDA 510(k) Cleared Devices
7
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Siemens-Pacesetter, Inc. Cardiovascular ✕
7 devices
Cleared
Aug 08, 1994
AFP CARDIAC PACING SYSTEM MODEL 283
Cardiovascular
80d
Cleared
Jul 15, 1994
PACING LEAD MODEL 1188T
Cardiovascular
648d
Cleared
Jul 06, 1994
PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS
Cardiovascular
387d
Cleared
Jun 15, 1994
SILICONE BIPOLAR LEAD MODELS 1136T, 1142T &1146T
Cardiovascular
481d
Cleared
Jun 10, 1993
MODEL 1148T TRANSVENOUS, SCREW-IN LEAD
Cardiovascular
231d
Cleared
Jan 22, 1993
CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE
Cardiovascular
333d
Cleared
Aug 03, 1992
ADAPTING SLEEVE KIT MODEL 4023
Cardiovascular
137d