510(k) K813135 ยท DTB Permanent Pacemaker Electrode
MODEL 486-01 PACEMAKER LEAD
| Applicant | Intermedics, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 3, 1985 |
| Received | Nov 5, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813135
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.