Vitatron Medical BV
Vitatron Medical BV holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1986.
Top product codes for Vitatron Medical BV
Recent clearances by Vitatron Medical BV
- K854790 — CERYX PACEMAKER MODELS 114, 314 & 614
- K844484 — HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA
- K844483 — TP 1
- K844485 — CERYX6, 611, CERYX 3 311 & CERYX 1 111
- K840668 — ELECTRODE PACEMAKER, PERM & TEMP
- K831859 — PACEMAKER PROGRAMMER #2032
- K831860 — GENERATOR, PULSE, PACEMAKER #532
- K810928 — ENDOCARDIAL ELECTRODE
- K791920 — CARDIAC PACEMAKER P4000 SER. & P1000
- K791921 — CARDIAC PACEMAKER C4000, C1000 SER.
- K791380 — VA 1000
- K790666 — VITALITH S 3000 SERIES
- K781168 — GENERATOR, PULSE, PACEMAKER
- K780717 — EXTERNAL TEST PULSE GENERATOR
- K772009 — CARDIAC PACEMAKER S6001
- K772010 — CARDIAC PACEMAKER C2001
- K760669 — PACEMAKERS, VITATRON'S
- K760670 — PACEMAKERS, VITATRONS (SERIES 2000)
- K760671 — PACEMAKERS, VITATRONS (SERIES 3000)
Data sourced from openFDA. This site is unofficial and independent of the FDA.