510(k) K896742 ยท DTB Permanent Pacemaker Electrode
FOCUS J81F, J83F, J41F, J43F PACING LEADS
| Applicant | Ela Medical, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jul 17, 1990 |
| Received | Nov 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896742
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.