510(k) K781208 ยท DXY Implantable Pacemaker Pulse-Generator
GENERATORS, PULSE, MODELS 5988/5989
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Oct 3, 1978 |
| Received | Jul 14, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781208
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.