510(k) K801416 ยท DTB Permanent Pacemaker Electrode
PACEPATH MODEL 810
| Applicant | Pacesetter Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 31, 1980 |
| Received | Jun 16, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801416
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.