510(k) K821518 ยท LDF Electrode, Pacemaker, Temporary
MYO/CLIP
| Applicant | Alto Development Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 8, 1982 |
| Received | May 21, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821518
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.