Company ยท US
Vitatron Medical BV
FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1986. Name variants (Inc, Corp, punctuation) are merged.
19510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 28, 1986 | K854790 | CERYX PACEMAKER MODELS 114, 314 & 614 Vitatron Medical BV | DXY |
| Jul 24, 1985 | K844484 | HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA Vitatron Medical BV, NL | KRG |
| Apr 19, 1985 | K844485 | CERYX6, 611, CERYX 3 311 & CERYX 1 111 Vitatron Medical BV, NL | KRG |
| Apr 19, 1985 | K844483 | TP 1 Vitatron Medical BV, NL | KRG |
| Sep 24, 1984 | K840668 | ELECTRODE PACEMAKER, PERM & TEMP Vitatron Medical BV | DTB |
| Oct 27, 1983 | K831860 | GENERATOR, PULSE, PACEMAKER #532 Vitatron Medical BV | DXY |
| Oct 27, 1983 | K831859 | PACEMAKER PROGRAMMER #2032 Vitatron Medical BV | DXY |
| Jul 2, 1981 | K810928 | ENDOCARDIAL ELECTRODE Vitatron Medical BV | DTB |
| Nov 29, 1979 | K791920 | CARDIAC PACEMAKER P4000 SER. & P1000 Vitatron Medical BV | DXY |
| Oct 26, 1979 | K791921 | CARDIAC PACEMAKER C4000, C1000 SER. Vitatron Medical BV | DXY |
| Sep 19, 1979 | K791380 | VA 1000 Vitatron Medical BV | DTA |
| Jun 1, 1979 | K790666 | VITALITH S 3000 SERIES Vitatron Medical BV | DXY |
| Aug 31, 1978 | K781168 | GENERATOR, PULSE, PACEMAKER Vitatron Medical BV | DXY |
| Jun 30, 1978 | K780717 | EXTERNAL TEST PULSE GENERATOR Vitatron Medical BV | DTC |
| Nov 28, 1977 | K772010 | CARDIAC PACEMAKER C2001 Vitatron Medical BV | DXY |
| Nov 28, 1977 | K772009 | CARDIAC PACEMAKER S6001 Vitatron Medical BV | DXY |
| Nov 12, 1976 | K760671 | PACEMAKERS, VITATRONS (SERIES 3000) Vitatron Medical BV | DXY |
| Nov 12, 1976 | K760670 | PACEMAKERS, VITATRONS (SERIES 2000) Vitatron Medical BV | DXY |
| Nov 12, 1976 | K760669 | PACEMAKERS, VITATRON'S Vitatron Medical BV | DXY |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||