510(k) K782018 ยท DTB Permanent Pacemaker Electrode
LEADS, IMPLANTABLE CARDIAC PACEMAKERS
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Jun 4, 1979 |
| Received | Dec 5, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782018
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.