510(k) K791768 ยท DTB Permanent Pacemaker Electrode
CORDIS PERMANENT PERVENOUS CARDIAC LEADS
| Applicant | Cordis Corp., Walker MI, US |
| Decision | Substantially Equivalent, Nov 5, 1979 |
| Received | Sep 5, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791768
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.