510(k) K780717 ยท DTC Analyzer, Pacemaker Generator Function
EXTERNAL TEST PULSE GENERATOR
| Applicant | Vitatron Medical BV, Walker MI, US |
| Decision | Substantially Equivalent, Jun 30, 1978 |
| Received | Apr 27, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780717
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.