510(k) K811876 ยท DTB Permanent Pacemaker Electrode
MODEL D BIPOLAR ENDOCARDIAL LEAD
| Applicant | Cook Pacemaker Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 3, 1981 |
| Received | Jul 1, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811876
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.