510(k) K821333 ยท LDF Electrode, Pacemaker, Temporary
ATRIAL J TEMPORARY PACING ELECTRODESS
| Applicant | Medics Instrument Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 2, 1982 |
| Received | May 5, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821333
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.