510(k) K883265 ยท DTB Permanent Pacemaker Electrode
MODEL 329-701 BIPOLAR ACTIVE-FIXATION LEAD
| Applicant | Telectronics and Cordis Pacing Systems, Englewood CO, US |
| Decision | Substantially Equivalent, Oct 14, 1988 |
| Received | Aug 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883265
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.