510(k) K790386 ยท DTB Permanent Pacemaker Electrode
LEAD MODELS MUM 1260, MUM 1290
| Applicant | Ela Medical, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 3, 1979 |
| Received | Feb 26, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790386
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.