510(k) K870034 ยท DTB Permanent Pacemaker Electrode
MODEL PY...U UNIPOLAR & BIPOLAR PACING LEAD
| Applicant | Oscor Medical Corp., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Mar 3, 1987 |
| Received | Jan 5, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870034
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.