510(k) K862330 ยท DTB Permanent Pacemaker Electrode
MODIFIED OSCOR PY PACING LEADS
| Applicant | Oscor Medical Corp., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Aug 8, 1986 |
| Received | Jun 19, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862330
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.