510(k) K895447 ยท DTB Permanent Pacemaker Electrode
ENDOCARDIAL SCREW-IN LEAD MODEL 1020T
| Applicant | Pacesetter Systems, Sylmar CA, US |
| Decision | Substantially Equivalent, Dec 20, 1989 |
| Received | Sep 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895447
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.