510(k) K874366 ยท DTB Permanent Pacemaker Electrode
ENCOR BIPOLAR ACT/FIXA LEAD W/POR SUR ELE #329-201
| Applicant | Cordis Leads, Inc., Suffield CT, US |
| Decision | Substantially Equivalent, Jun 16, 1988 |
| Received | Oct 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874366
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.