510(k) K832850 ยท LDF Electrode, Pacemaker, Temporary
ELECATH PACEWEDGE DUAL PRESS. BIPOLAR
| Applicant | Electro-Catheter Corp., Walker MI, US |
| Decision | Substantially Equivalent, Oct 19, 1983 |
| Received | Aug 22, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832850
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.