510(k) K971474 ยท DTE Pulse-Generator, Pacemaker, External
MEDTRONIC MODEL 5318 TEMPORARY PACEMAKER/IMPLANT TOOL
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 14, 1997 |
| Received | Apr 23, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971474
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.