510(k) K875178 ยท DTB Permanent Pacemaker Electrode
MODEL 435-04 CARDIFIX SIDE HOOK IMPLANT. PACE LEAD
| Applicant | Intermedics, Inc., Freeport TX, US |
| Decision | Substantially Equivalent, May 25, 1988 |
| Received | Dec 17, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875178
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.