Vitatron Medical BV is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vitatron Medical BV - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Vitatron Medical BV has 19 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1976 to 1986.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vitatron Medical BV
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