# Vitatron Medical BV

- Location (FDA's records): Mchenry, IL
- FDA decisions: 19 (1976–1986): 19 510(k) clearances
- Product codes: DXY (12), KRG (3), DTB (2), DTA (1), DTC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K854790: Ceryx Pacemaker Models 114, 314 & 614 (Aug 28, 1986)
- K844484: Hewlett Packardt HP 85 W/ Vitatron PH1 Program Hea (Jul 24, 1985)
- K844483: TP 1 (Apr 19, 1985)
- K844485: CERYX6, 611, Ceryx 3 311 & Ceryx 1 111 (Apr 19, 1985)
- K840668: Electrode Pacemaker, Perm & Temp (Sep 24, 1984)
- K831859: Pacemaker Programmer #2032 (Oct 27, 1983)
- K831860: Generator, Pulse, Pacemaker #532 (Oct 27, 1983)
- K810928: Endocardial Electrode (Jul 2, 1981)

Source page: https://510kreport.com/company/vitatron-medical