510(k) K890018 ยท DTB Permanent Pacemaker Electrode
PACEMAKER LEAD ADAPTER
| Applicant | Ela Medical, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jun 20, 1989 |
| Received | Jan 3, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890018
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.