510(k) K872972 ยท LDF Electrode, Pacemaker, Temporary
TEMPORARY PACEMAKER ELECTRODE
| Applicant | Oscor Medical Corp., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Dec 3, 1987 |
| Received | Jul 29, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872972
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.