510(k) K802294 ยท DTB Permanent Pacemaker Electrode
POLY FLEX IMPLANTABLE PACING LEAD
| Applicant | Intermedics, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 3, 1985 |
| Received | Sep 19, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802294
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.