510(k) K782108 ยท DTE Pulse-Generator, Pacemaker, External
MEDTRONIC MODEL 546
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Dec 29, 1978 |
| Received | Dec 19, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782108
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.