510(k) K823891 ยท DTB Permanent Pacemaker Electrode
MODEL KY PACEMAKER LEAD - VARIOUS
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Mar 31, 1983 |
| Received | Dec 27, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823891
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.