510(k) K820003 ยท LDF Electrode, Pacemaker, Temporary
CARDIOVASCULAR TEMP. PACEMAKER ELEC
| Applicant | Diag Corp., Walker MI, US |
| Decision | Substantially Equivalent, Mar 26, 1982 |
| Received | Jan 4, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820003
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.