Vitatron Medical BV - FDA 510(k) Cleared Devices
Recent clearances: CERYX PACEMAKER MODELS 114, 314 & 614, HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA, TP 1
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vitatron Medical BV Cardiovascular ✕
19 devices
Cleared
Aug 28, 1986
CERYX PACEMAKER MODELS 114, 314 & 614
Cardiovascular
272d
Cleared
Jul 24, 1985
HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA
Cardiovascular
247d
Cleared
Apr 19, 1985
TP 1
Cardiovascular
151d
Cleared
Apr 19, 1985
CERYX6, 611, CERYX 3 311 & CERYX 1 111
Cardiovascular
151d
Cleared
Sep 24, 1984
ELECTRODE PACEMAKER, PERM & TEMP
Cardiovascular
237d
Cleared
Oct 27, 1983
PACEMAKER PROGRAMMER #2032
Cardiovascular
139d
Cleared
Oct 27, 1983
GENERATOR, PULSE, PACEMAKER #532
Cardiovascular
139d
Cleared
Jul 02, 1981
ENDOCARDIAL ELECTRODE
Cardiovascular
87d
Cleared
Nov 29, 1979
CARDIAC PACEMAKER P4000 SER. & P1000
Cardiovascular
65d
Cleared
Oct 26, 1979
CARDIAC PACEMAKER C4000, C1000 SER.
Cardiovascular
31d
Cleared
Sep 19, 1979
VA 1000
Cardiovascular
57d
Cleared
Jun 01, 1979
VITALITH S 3000 SERIES
Cardiovascular
56d