510(k) K880551 ยท DTB Permanent Pacemaker Electrode
MODEL 439-07 AND 439-09 LIFELINE MYOCARDIAL LEAD
| Applicant | Intermedics, Inc., Freeport TX, US |
| Decision | Substantially Equivalent, Mar 7, 1988 |
| Received | Feb 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880551
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.