510(k) K873962 ยท DTB Permanent Pacemaker Electrode
MEDTRONIC MODEL 4016A ENDOCARDIAL PACING LEAD
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 2, 1988 |
| Received | Sep 29, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873962
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.