510(k) K810139 ยท DTB Permanent Pacemaker Electrode
ELECTRODE, PACEMAKER, PERMANENT
| Applicant | Pacesetter Systems, Walker MI, US |
| Decision | Substantially Equivalent, Nov 27, 1981 |
| Received | Jan 21, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810139
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.