510(k) K810202 ยท DTB Permanent Pacemaker Electrode
CORDIS MULTIFILAR PERVENOUS VENTRIC. LD
| Applicant | Cordis Corp., Walker MI, US |
| Decision | Substantially Equivalent, Feb 5, 1981 |
| Received | Jan 23, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810202
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.