510(k) K821889 ยท DTB Permanent Pacemaker Electrode
POROUS SURFACED PLATINUM IRIDIUM
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 6, 1982 |
| Received | Jun 25, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821889
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.