510(k) K830772 ยท LDF Electrode, Pacemaker, Temporary
TEMP. PACING LEAD, BIPOLAR #TH60, 90/110
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Apr 18, 1983 |
| Received | Mar 11, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830772
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.